ClinVar for Gene (Select 144132) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3084762	NM_144666.3(DNHD1):c.9797A>G (p.His3266Arg)	DNHD1 (H3266R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3084761	NM_144666.3(DNHD1):c.9740G>C (p.Arg3247Pro)	DNHD1 (R3247P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084760	NM_144666.3(DNHD1):c.9650G>A (p.Arg3217Gln)	DNHD1 (R3217Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3084759	NM_144666.3(DNHD1):c.9629G>A (p.Arg3210Gln)	DNHD1 (R3210Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084758	NM_144666.3(DNHD1):c.9608T>A (p.Ile3203Asn)	DNHD1 (I3203N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084757	NM_144666.3(DNHD1):c.95A>G (p.Lys32Arg)	DNHD1 (K32R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084756	NM_144666.3(DNHD1):c.9553A>G (p.Ser3185Gly)	DNHD1 (S3185G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084755	NM_144666.3(DNHD1):c.9299A>G (p.His3100Arg)	DNHD1 (H3100R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084754	NM_144666.3(DNHD1):c.9106C>G (p.Leu3036Val)	DNHD1 (L3036V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084753	NM_144666.3(DNHD1):c.8932A>G (p.Ile2978Val)	DNHD1 (I2978V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084751	NM_144666.3(DNHD1):c.8686G>A (p.Gly2896Arg)	DNHD1 (G2896R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084750	NM_144666.3(DNHD1):c.8678T>C (p.Leu2893Pro)	DNHD1 (L2893P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084749	NM_144666.3(DNHD1):c.8648G>A (p.Arg2883Gln)	DNHD1 (R2883Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084748	NM_144666.3(DNHD1):c.8509T>C (p.Tyr2837His)	DNHD1 (Y2837H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084747	NM_144666.3(DNHD1):c.8279T>C (p.Met2760Thr)	DNHD1 (M2760T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3084746	NM_144666.3(DNHD1):c.8156A>T (p.Asp2719Val)	DNHD1 (D2719V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084745	NM_144666.3(DNHD1):c.8101G>C (p.Glu2701Gln)	DNHD1 (E2701Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084744	NM_144666.3(DNHD1):c.80G>A (p.Cys27Tyr)	DNHD1 (C27Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084743	NM_144666.3(DNHD1):c.7980C>G (p.Asp2660Glu)	DNHD1 (D2660E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084742	NM_144666.3(DNHD1):c.7941G>T (p.Trp2647Cys)	DNHD1 (W2647C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084741	NM_144666.3(DNHD1):c.7757A>T (p.His2586Leu)	DNHD1 (H2586L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084740	NM_144666.3(DNHD1):c.7690G>C (p.Val2564Leu)	DNHD1 (V2564L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084739	NM_144666.3(DNHD1):c.7663C>T (p.Arg2555Trp)	DNHD1 (R2555W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084738	NM_144666.3(DNHD1):c.7630C>A (p.Gln2544Lys)	DNHD1 (Q2544K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084737	NM_144666.3(DNHD1):c.7534C>T (p.Arg2512Cys)	DNHD1 (R2512C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084736	NM_144666.3(DNHD1):c.7009C>A (p.Pro2337Thr)	DNHD1 (P2337T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084735	NM_144666.3(DNHD1):c.6876C>G (p.Ile2292Met)	DNHD1 (I2292M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084734	NM_144666.3(DNHD1):c.682G>A (p.Val228Ile)	DNHD1 (V228I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084733	NM_144666.3(DNHD1):c.6809G>A (p.Ser2270Asn)	DNHD1 (S2270N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084732	NM_144666.3(DNHD1):c.67T>A (p.Trp23Arg)	DNHD1 (W23R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084731	NM_144666.3(DNHD1):c.6656G>A (p.Ser2219Asn)	DNHD1 (S2219N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084730	NM_144666.3(DNHD1):c.6640G>A (p.Val2214Met)	DNHD1 (V2214M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084729	NM_144666.3(DNHD1):c.6610G>T (p.Val2204Leu)	DNHD1 (V2204L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084728	NM_144666.3(DNHD1):c.6518G>A (p.Arg2173Gln)	DNHD1 (R2173Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3084727	NM_144666.3(DNHD1):c.64T>G (p.Ser22Ala)	DNHD1 (S22A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084726	NM_144666.3(DNHD1):c.6171G>C (p.Lys2057Asn)	DNHD1 (K2057N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084725	NM_144666.3(DNHD1):c.6073C>A (p.Pro2025Thr)	DNHD1 (P2025T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084724	NM_144666.3(DNHD1):c.5951G>A (p.Arg1984Gln)	DNHD1 (R1984Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3084723	NM_144666.3(DNHD1):c.5890G>A (p.Gly1964Ser)	DNHD1 (G1964S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084722	NM_144666.3(DNHD1):c.5810C>G (p.Pro1937Arg)	DNHD1 (P1937R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084721	NM_144666.3(DNHD1):c.5683C>G (p.Pro1895Ala)	DNHD1 (P1895A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084720	NM_144666.3(DNHD1):c.5383G>A (p.Val1795Met)	DNHD1 (V1795M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084719	NM_144666.3(DNHD1):c.5168G>A (p.Ser1723Asn)	DNHD1 (S1723N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084718	NM_144666.3(DNHD1):c.5116C>T (p.Arg1706Cys)	DNHD1 (R1706C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084717	NM_144666.3(DNHD1):c.4868T>G (p.Leu1623Arg)	DNHD1 (L1623R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084716	NM_144666.3(DNHD1):c.4745G>A (p.Arg1582Gln)	DNHD1 (R1582Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084715	NM_144666.3(DNHD1):c.4408C>T (p.Arg1470Cys)	DNHD1 (R1470C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084714	NM_144666.3(DNHD1):c.4324C>T (p.Pro1442Ser)	DNHD1 (P1442S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084713	NM_144666.3(DNHD1):c.430G>A (p.Ala144Thr)	DNHD1 (A144T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084712	NM_144666.3(DNHD1):c.4166C>T (p.Pro1389Leu)	DNHD1 (P1389L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084711	NM_144666.3(DNHD1):c.4042G>A (p.Val1348Met)	DNHD1 (V1348M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084710	NM_144666.3(DNHD1):c.3956G>A (p.Ser1319Asn)	DNHD1 (S1319N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084709	NM_144666.3(DNHD1):c.3849C>G (p.Asp1283Glu)	DNHD1 (D1283E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3084708	NM_144666.3(DNHD1):c.3575G>A (p.Arg1192His)	DNHD1 (R1192H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084707	NM_144666.3(DNHD1):c.3460A>T (p.Thr1154Ser)	DNHD1 (T1154S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084706	NM_144666.3(DNHD1):c.3410G>A (p.Arg1137Gln)	DNHD1 (R1137Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084705	NM_144666.3(DNHD1):c.3186G>A (p.Met1062Ile)	DNHD1 (M1062I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084704	NM_144666.3(DNHD1):c.308A>T (p.Asp103Val)	DNHD1 (D103V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084703	NM_144666.3(DNHD1):c.3041C>G (p.Pro1014Arg)	DNHD1 (P1014R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084702	NM_144666.3(DNHD1):c.3038G>A (p.Arg1013His)	DNHD1 (R1013H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084701	NM_144666.3(DNHD1):c.2647G>A (p.Gly883Arg)	DNHD1 (G883R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3084700	NM_144666.3(DNHD1):c.2402G>A (p.Cys801Tyr)	DNHD1 (C801Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084699	NM_144666.3(DNHD1):c.2327A>G (p.His776Arg)	DNHD1 (H776R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3084698	NM_144666.3(DNHD1):c.2287G>A (p.Glu763Lys)	DNHD1 (E763K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084697	NM_144666.3(DNHD1):c.2173C>A (p.Gln725Lys)	DNHD1 (Q725K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084696	NM_144666.3(DNHD1):c.2117A>G (p.Lys706Arg)	DNHD1 (K706R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084695	NM_144666.3(DNHD1):c.2021A>G (p.His674Arg)	DNHD1 (H674R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3084694	NM_144666.3(DNHD1):c.1966A>G (p.Ile656Val)	DNHD1 (I656V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084693	NM_144666.3(DNHD1):c.1712A>G (p.His571Arg)	DNHD1 (H571R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084692	NM_144666.3(DNHD1):c.1432G>A (p.Glu478Lys)	DNHD1 (E478K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084691	NM_144666.3(DNHD1):c.14003G>A (p.Gly4668Glu)	DNHD1 (G4668E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084689	NM_144666.3(DNHD1):c.13777C>G (p.Leu4593Val)	DNHD1 (L4593V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084688	NM_144666.3(DNHD1):c.13734G>C (p.Glu4578Asp)	DNHD1 (E4578D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084687	NM_144666.3(DNHD1):c.13714G>A (p.Ala4572Thr)	DNHD1 (A4572T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084685	NM_144666.3(DNHD1):c.1346G>A (p.Arg449Gln)	DNHD1 (R449Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084684	NM_144666.3(DNHD1):c.13150C>T (p.His4384Tyr)	DNHD1 (H4384Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084683	NM_144666.3(DNHD1):c.12674A>C (p.Gln4225Pro)	DNHD1 (Q4225P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084682	NM_144666.3(DNHD1):c.12040C>A (p.Gln4014Lys)	DNHD1 (Q4014K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084681	NM_144666.3(DNHD1):c.11962C>T (p.His3988Tyr)	DNHD1 (H3988Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084680	NM_144666.3(DNHD1):c.11729T>C (p.Leu3910Ser)	DNHD1 (L3910S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084679	NM_144666.3(DNHD1):c.11578A>G (p.Met3860Val)	DNHD1 (M3860V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084677	NM_144666.3(DNHD1):c.11390G>A (p.Arg3797Gln)	DNHD1 (R3797Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3084676	NM_144666.3(DNHD1):c.11269C>A (p.Leu3757Met)	DNHD1 (L3757M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084675	NM_144666.3(DNHD1):c.11033T>A (p.Leu3678His)	DNHD1 (L3678H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084674	NM_144666.3(DNHD1):c.11024G>A (p.Gly3675Asp)	DNHD1 (G3675D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084673	NM_144666.3(DNHD1):c.11011G>A (p.Asp3671Asn)	DNHD1 (D3671N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084671	NM_144666.3(DNHD1):c.10898A>T (p.Glu3633Val)	DNHD1 (E3633V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084670	NM_144666.3(DNHD1):c.10789A>G (p.Ser3597Gly)	DNHD1 (S3597G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084669	NM_144666.3(DNHD1):c.10570G>A (p.Asp3524Asn)	DNHD1 (D3524N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084668	NM_144666.3(DNHD1):c.10556A>C (p.Glu3519Ala)	DNHD1 (E3519A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084667	NM_144666.3(DNHD1):c.10519C>G (p.Pro3507Ala)	DNHD1 (P3507A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084666	NM_144666.3(DNHD1):c.10253C>T (p.Thr3418Met)	DNHD1 (T3418M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3084664	NM_144666.3(DNHD1):c.10076G>A (p.Arg3359Gln)	DNHD1 (R3359Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084663	NM_144666.3(DNHD1):c.10024C>T (p.Arg3342Trp)	DNHD1 (R3342W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084662	NM_144666.3(DNHD1):c.10006T>G (p.Tyr3336Asp)	DNHD1 (Y3336D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3067354	NM_144666.3(DNHD1):c.14020C>G (p.Pro4674Ala)	DNHD1 (P4674A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3065700	NM_144666.3(DNHD1):c.1236-1G>A	DNHD1	Single nucleotide variant (splice acceptor variant)	Spermatogenic failure 65	GUncertain significance
Select item 3064742	NM_144666.3(DNHD1):c.7831C>T (p.Arg2611Ter)	DNHD1 (R2611*)	Single nucleotide variant (nonsense)	Spermatogenic failure 65	GLikely pathogenic
Select item 3064044	NM_144666.3(DNHD1):c.1324G>A (p.Glu442Lys)	DNHD1 (E442K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3064043	NM_144666.3(DNHD1):c.6814G>A (p.Asp2272Asn)	DNHD1 (D2272N)	Single nucleotide variant (missense variant)	not provided	Gnot provided

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