TAF7L[gene] and "single gene"[properties] - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2524041	NM_001168474.2(TAF7L):c.1127A>G (p.Lys376Arg)	TAF7L (K376R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1205846	NM_001168474.2(TAF7L):c.1115G>A (p.Arg372His)	TAF7L (R372H +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2588076	NM_001168474.2(TAF7L):c.1102G>A (p.Glu368Lys)	TAF7L (E368K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173583	NM_001168474.2(TAF7L):c.713T>C (p.Met238Thr)	TAF7L (M324T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3324290	NM_001168474.2(TAF7L):c.706C>T (p.Arg236Trp)	TAF7L (R322W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335776	NM_001168474.2(TAF7L):c.676G>A (p.Gly226Ser)	TAF7L (G312S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595011	NM_001168474.2(TAF7L):c.653C>T (p.Ser218Leu)	TAF7L (S218L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588077	NM_001168474.2(TAF7L):c.645G>T (p.Leu215Phe)	TAF7L (L215F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401946	NM_001168474.2(TAF7L):c.608A>G (p.Lys203Arg)	TAF7L (K203R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324289	NM_001168474.2(TAF7L):c.607A>G (p.Lys203Glu)	TAF7L (K203E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3173582	NM_001168474.2(TAF7L):c.595G>A (p.Glu199Lys)	TAF7L (E285K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324288	NM_001168474.2(TAF7L):c.568G>A (p.Val190Ile)	TAF7L (V276I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2351324	NM_001168474.2(TAF7L):c.551G>A (p.Arg184His)	TAF7L (R270H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482891	NM_001168474.2(TAF7L):c.523G>A (p.Val175Met)	TAF7L (V175M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777798	NM_001168474.2(TAF7L):c.375G>A (p.Gly125=)	TAF7L	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2593746	NM_001168474.2(TAF7L):c.361A>G (p.Lys121Glu)	TAF7L (K121E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3324287	NM_001168474.2(TAF7L):c.352A>G (p.Ile118Val)	TAF7L (I204V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2355721	NM_001168474.2(TAF7L):c.236C>T (p.Thr79Met)	TAF7L (T165M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597619	NM_001168474.2(TAF7L):c.97C>T (p.Arg33Cys)	TAF7L (R119C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527194	NM_001168474.2(TAF7L):c.17A>G (p.Asp6Gly)	TAF7L (D6G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 624435	NM_001168474.2(TAF7L):c.14A>G (p.Gln5Arg)	TAF7L (Q91R +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2280092	NM_024885.4(TAF7L):c.232C>T (p.Pro78Ser)	TAF7L (P78S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 100877	NM_024885.4(TAF7L):c.213C>T (p.Ala71=)	TAF7L	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 785704	NM_024885.4(TAF7L):c.210C>T (p.Ser70=)	TAF7L	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 788756	NM_024885.4(TAF7L):c.181G>A (p.Glu61Lys)	TAF7L (E61K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2602089	NM_024885.4(TAF7L):c.154G>A (p.Asp52Asn)	TAF7L (D52N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459930	NM_024885.4(TAF7L):c.128A>G (p.Tyr43Cys)	TAF7L (Y43C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2516040	NM_024885.4(TAF7L):c.106G>T (p.Asp36Tyr)	TAF7L (D36Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 28