"PreventionGenetics, part of Exact Sciences"[submitter] AND "PRDM13"[g - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3060623	NC_000006.12:g.99598936A>C	PRDM13	Single nucleotide variant	PRDM13-related condition	GLikely benign
Select item 1575042	NM_021620.4(PRDM13):c.147G>A (p.Val49=)	PRDM13	Single nucleotide variant (synonymous variant)	PRDM13-related condition +1 more	GLikely benign
Select item 1167633	NM_021620.4(PRDM13):c.488G>C (p.Ser163Thr)	PRDM13 (S163T)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1169310	NM_021620.4(PRDM13):c.639G>A (p.Leu213=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1170888	NM_021620.4(PRDM13):c.710C>T (p.Ala237Val)	PRDM13 (A237V)	Single nucleotide variant (missense variant)	PRDM13-related condition +1 more	GBenign/Likely benign
Select item 1164417	NM_021620.4(PRDM13):c.864C>T (p.Tyr288=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3037903	NM_021620.4(PRDM13):c.900A>C (p.Leu300=)	PRDM13	Single nucleotide variant (synonymous variant)	PRDM13-related condition	GLikely benign
Select item 3037290	NM_021620.4(PRDM13):c.903G>T (p.Ala301=)	PRDM13	Single nucleotide variant (synonymous variant)	PRDM13-related condition	GLikely benign
Select item 1091407	NM_021620.4(PRDM13):c.972C>G (p.Leu324=)	LOC129996881, PRDM13	Single nucleotide variant (synonymous variant)	PRDM13-related condition +1 more	GLikely benign
Select item 1159149	NM_021620.4(PRDM13):c.1283G>C (p.Gly428Ala)	PRDM13 (G428A)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 726858	NM_021620.4(PRDM13):c.1374C>A (p.Val458=)	PRDM13	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 844237	NM_021620.4(PRDM13):c.1813G>A (p.Val605Ile)	PRDM13 (V605I)	Single nucleotide variant (missense variant)	PRDM13-related condition +1 more	GUncertain significance