"PreventionGenetics, part of Exact Sciences"[submitter] AND "WDR37"[ge - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3045494	NM_014023.4(WDR37):c.105G>A (p.Arg35=)	WDR37	Single nucleotide variant (synonymous variant)	WDR37-related disorder	GLikely benign
Select item 3054836	NM_014023.4(WDR37):c.138+10G>A	WDR37	Single nucleotide variant (intron variant)	WDR37-related disorder	GLikely benign
Select item 3052520	NM_014023.4(WDR37):c.175C>G (p.Leu59Val)	WDR37 (L59V)	Single nucleotide variant (missense variant)	WDR37-related disorder	GUncertain significance
Select item 2640272	NM_014023.4(WDR37):c.212A>G (p.Asn71Ser)	WDR37 (N71S)	Single nucleotide variant (missense variant)	WDR37-related disorder +1 more	GBenign/Likely benign
Select item 2629090	NM_014023.4(WDR37):c.311A>G (p.Lys104Arg)	WDR37 (K104R)	Single nucleotide variant (missense variant)	WDR37-related disorder	GUncertain significance
Select item 2640273	NM_014023.4(WDR37):c.363A>G (p.Lys121=)	WDR37	Single nucleotide variant (synonymous variant)	WDR37-related disorder +1 more	GBenign/Likely benign
Select item 440948	NM_014023.4(WDR37):c.374C>T (p.Thr125Ile)	WDR37 (T125I)	Single nucleotide variant (missense variant)	WDR37-related disorder +7 more	GPathogenic/Likely pathogenic
Select item 2629390	NM_014023.4(WDR37):c.419C>T (p.Thr140Met)	WDR37 (T140M)	Single nucleotide variant (missense variant)	WDR37-related disorder	GUncertain significance
Select item 3054333	NM_014023.4(WDR37):c.429A>G (p.Arg143=)	WDR37	Single nucleotide variant (synonymous variant)	WDR37-related disorder	GLikely benign
Select item 2640274	NM_014023.4(WDR37):c.531C>T (p.Ala177=)	WDR37	Single nucleotide variant (synonymous variant)	WDR37-related disorder +1 more	GBenign/Likely benign
Select item 2635533	NM_014023.4(WDR37):c.829C>T (p.Leu277Phe)	WDR37 (L277F)	Single nucleotide variant (missense variant)	WDR37-related disorder	GUncertain significance
Select item 3044266	NM_014023.4(WDR37):c.963G>T (p.Gly321=)	WDR37	Single nucleotide variant (synonymous variant)	WDR37-related disorder	GLikely benign
Select item 1690599	NM_014023.4(WDR37):c.1103+10G>A	WDR37	Single nucleotide variant (intron variant)	See cases +1 more	GConflicting classifications of pathogenicity
Select item 3036850	NM_014023.4(WDR37):c.1155C>T (p.Ser385=)	WDR37	Single nucleotide variant (synonymous variant)	WDR37-related disorder	GLikely benign
Select item 2632400	NM_014023.4(WDR37):c.1156G>T (p.Asp386Tyr)	WDR37 (D386Y)	Single nucleotide variant (missense variant)	WDR37-related disorder	GUncertain significance
Select item 3043959	NM_014023.4(WDR37):c.1239-9T>A	WDR37	Single nucleotide variant (intron variant)	WDR37-related disorder	GLikely benign
Select item 3049719	NM_014023.4(WDR37):c.1383A>G (p.Ala461=)	WDR37	Single nucleotide variant (synonymous variant)	WDR37-related disorder	GLikely benign