Related gene-specific medical variations for Gene (Select 5793) - ClinVar

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Links from Gene

Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3025815	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 3024706	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 2685923	GRCh37/hg19 3p14.2(chr3:61326494-61627053)x3	PTPRG	Copy number gain	not provided	GUncertain significance
Select item 2685922	GRCh37/hg19 3p14.2(chr3:61306671-61819114)x3	PTPRG	Copy number gain	not provided	GUncertain significance
Select item 2653933	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 2653932	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 2653931	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 2653930	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 2653929	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 2653928	NM_002841.4(PTPRG):c.3766-12_3766-11insTTTTTTTTTTTTTTTTTTTT	PTPRG, PTPRG-AS1	Insertion (intron variant)	not provided	GLikely benign
Select item 2616013	NM_002841.4(PTPRG):c.4207A>G (p.Ile1403Val)	PTPRG, PTPRG-AS1 (I1403V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2554709	NM_002841.4(PTPRG):c.3710T>C (p.Met1237Thr)	PTPRG, PTPRG-AS1 (M1208T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2545420	NM_002841.4(PTPRG):c.3181A>G (p.Ser1061Gly)	PTPRG, PTPRG-AS1 (S1032G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2486659	NM_002841.4(PTPRG):c.2681G>T (p.Arg894Ile)	PTPRG, PTPRG-AS1 (R865I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2401595	NM_002841.4(PTPRG):c.3431T>G (p.Val1144Gly)	PTPRG-AS1, PTPRG (V1115G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2393798	NM_002841.4(PTPRG):c.3964C>G (p.Pro1322Ala)	PTPRG, PTPRG-AS1 (P1293A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2390151	NM_002841.4(PTPRG):c.3566G>A (p.Arg1189His)	PTPRG, PTPRG-AS1 (R1160H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2388880	NM_002841.4(PTPRG):c.3401G>A (p.Ser1134Asn)	PTPRG-AS1, PTPRG (S1105N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2387235	NM_002841.4(PTPRG):c.3211A>G (p.Ile1071Val)	PTPRG-AS1, PTPRG (I1042V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2385356	NM_002841.4(PTPRG):c.3974C>G (p.Pro1325Arg)	PTPRG-AS1, PTPRG (P1325R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2378066	NM_002841.4(PTPRG):c.3998T>C (p.Ile1333Thr)	PTPRG-AS1, PTPRG (I1304T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2361628	NM_002841.4(PTPRG):c.2570G>A (p.Arg857His)	PTPRG, PTPRG-AS1 (R828H +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2359414	NM_002841.4(PTPRG):c.4093A>G (p.Thr1365Ala)	PTPRG-AS1, PTPRG (T1336A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2348758	NM_002841.4(PTPRG):c.4003G>A (p.Val1335Ile)	PTPRG, PTPRG-AS1 (V1335I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2343044	NM_002841.4(PTPRG):c.3722A>G (p.His1241Arg)	PTPRG, PTPRG-AS1 (H1212R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2335757	NM_002841.4(PTPRG):c.4292T>C (p.Ile1431Thr)	PTPRG, PTPRG-AS1 (I1402T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2333345	NM_002841.4(PTPRG):c.3294G>C (p.Gln1098His)	PTPRG, PTPRG-AS1 (Q1098H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2322175	NM_002841.4(PTPRG):c.3728C>T (p.Ala1243Val)	PTPRG, PTPRG-AS1 (A1214V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2315034	NM_002841.4(PTPRG):c.4220T>A (p.Met1407Lys)	PTPRG-AS1, PTPRG (M1378K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2301508	NM_002841.4(PTPRG):c.3605G>A (p.Gly1202Glu)	PTPRG-AS1, PTPRG (G1173E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2288383	NM_002841.4(PTPRG):c.3116T>C (p.Leu1039Pro)	PTPRG, PTPRG-AS1 (L1010P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2279445	NM_002841.4(PTPRG):c.4049A>G (p.His1350Arg)	PTPRG, PTPRG-AS1 (H1350R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2278877	NM_002841.4(PTPRG):c.2809A>G (p.Arg937Gly)	PTPRG-AS1, PTPRG (R908G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2223061	NM_002841.4(PTPRG):c.3035G>A (p.Arg1012His)	PTPRG-AS1, PTPRG (R1012H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2208476	NM_002841.4(PTPRG):c.2936C>T (p.Thr979Met)	PTPRG-AS1, PTPRG (T979M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 713937	NM_002841.4(PTPRG):c.3262G>A (p.Val1088Ile)	PTPRG, PTPRG-AS1 (V1088I +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign

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Links from Gene

Items: 40