Related gene-specific medical variations for Gene (Select 83657) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2486977	NM_130897.3(DYNLRB2):c.152T>C (p.Met51Thr)	DYNLRB2, DYNLRB2-AS1 (M51T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2485837	NM_130897.3(DYNLRB2):c.200C>A (p.Thr67Asn)	DYNLRB2, DYNLRB2-AS1 (T67N +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2468283	NM_130897.3(DYNLRB2):c.179T>C (p.Ile60Thr)	DYNLRB2, DYNLRB2-AS1 (I89T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2456880	NM_130897.3(DYNLRB2):c.107A>C (p.Asn36Thr)	DYNLRB2, DYNLRB2-AS1 (N65T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2264715	NM_130897.3(DYNLRB2):c.253G>A (p.Glu85Lys)	DYNLRB2-AS1, DYNLRB2 (E114K +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2246054	NM_130897.3(DYNLRB2):c.192C>A (p.Asn64Lys)	DYNLRB2-AS1, DYNLRB2 (N93K +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2223941	NM_130897.3(DYNLRB2):c.173G>A (p.Arg58His)	DYNLRB2, DYNLRB2-AS1 (R87H +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2223922	NM_130897.3(DYNLRB2):c.268G>C (p.Val90Leu)	DYNLRB2-AS1, DYNLRB2 (V90L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2222720	NM_130897.3(DYNLRB2):c.220A>G (p.Lys74Glu)	DYNLRB2-AS1, DYNLRB2 (K103E +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 402815	NM_130897.3(DYNLRB2):c.196C>T (p.Leu66=)	DYNLRB2, DYNLRB2-AS1	Single nucleotide variant (synonymous variant +1 more)	not specified	GBenign