Product Details

SNP ID

rs140954606

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:47447575 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATTATCTGATGCATACTTAGTGTG[A/G]CTTTCTGGATGAAAGCTTTCCCACA

Phenotype

MIM: 314995

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ZNF41 PubMed Links

Gene Details

Gene

ZNF41

Gene Name

zinc finger protein 41

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001324139.1	2962	Missense Mutation	GCC,GTC	A646V	NP_001311068.1
NM_001324140.1	2962	Missense Mutation	GCC,GTC	A732V	NP_001311069.1
NM_001324141.1	2962	Missense Mutation	GCC,GTC	A646V	NP_001311070.1
NM_001324142.1	2962	Missense Mutation	GCC,GTC	A734V	NP_001311071.1
NM_001324143.1	2962	Missense Mutation	GCC,GTC	A646V	NP_001311072.1
NM_001324144.1	2962	Missense Mutation	GCC,GTC	A732V	NP_001311073.1
NM_001324145.1	2962	Missense Mutation	GCC,GTC	A646V	NP_001311074.1
NM_001324147.1	2962	Missense Mutation	GCC,GTC	A732V	NP_001311076.1
NM_001324148.1	2962	Missense Mutation	GCC,GTC	A734V	NP_001311077.1
NM_001324149.1	2962	Missense Mutation	GCC,GTC	A646V	NP_001311078.1
NM_001324150.1	2962	Missense Mutation	GCC,GTC	A732V	NP_001311079.1
NM_001324151.1	2962	Missense Mutation	GCC,GTC	A742V	NP_001311080.1
NM_001324152.1	2962	Missense Mutation	GCC,GTC	A646V	NP_001311081.1
NM_001324153.1	2962	Missense Mutation	GCC,GTC	A742V	NP_001311082.1
NM_001324154.1	2962	Missense Mutation	GCC,GTC	A766V	NP_001311083.1
NM_001324155.1	2962	Missense Mutation	GCC,GTC	A774V	NP_001311084.1
NM_001324156.1	2962	Missense Mutation	GCC,GTC	A698V	NP_001311085.1
NM_001324157.1	2962	Missense Mutation	GCC,GTC	A696V	NP_001311086.1
NM_007130.3	2962	Missense Mutation	GCC,GTC	A732V	NP_009061.1
NM_153380.3	2962	Missense Mutation	GCC,GTC	A732V	NP_700359.1
XM_006724550.3	2962	Missense Mutation	GCC,GTC	A766V	XP_006724613.1
XM_006724555.3	2962	Missense Mutation	GCC,GTC	A742V	XP_006724618.1
XM_017029810.1	2962	Missense Mutation	GCC,GTC	A766V	XP_016885299.1
XM_017029811.1	2962	Missense Mutation	GCC,GTC	A766V	XP_016885300.1
XM_017029812.1	2962	Missense Mutation	GCC,GTC	A766V	XP_016885301.1
XM_017029813.1	2962	Missense Mutation	GCC,GTC	A766V	XP_016885302.1
XM_017029814.1	2962	Missense Mutation	GCC,GTC	A766V	XP_016885303.1
XM_017029815.1	2962	Missense Mutation	GCC,GTC	A766V	XP_016885304.1
XM_017029816.1	2962	Missense Mutation	GCC,GTC	A742V	XP_016885305.1
XM_017029817.1	2962	Missense Mutation	GCC,GTC	A732V	XP_016885306.1

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