Product Details

SNP ID

rs192990608

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:85255589 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCGTGGCTGACCTTGTTACTGGTC[C/T]TAATGGACACTTAGAACATGTGGTC

Phenotype

MIM: 314990

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ZNF711 PubMed Links

Gene Details

Gene

ZNF711

Gene Name

zinc finger protein 711

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021998.4	637	Missense Mutation	CCT,CTT	P137L	NP_068838.3
XM_005262186.2	637	Missense Mutation	CCT,CTT	P137L	XP_005262243.1
XM_005262187.1	637	Missense Mutation	CCT,CTT	P137L	XP_005262244.1
XM_005262188.1	637	Missense Mutation	CCT,CTT	P137L	XP_005262245.1
XM_005262189.2	637	Missense Mutation	CCT,CTT	P137L	XP_005262246.1
XM_011531019.1	637	Missense Mutation	CCT,CTT	P141L	XP_011529321.1
XM_011531020.1	637	Missense Mutation	CCT,CTT	P141L	XP_011529322.1
XM_011531021.1	637	Missense Mutation	CCT,CTT	P141L	XP_011529323.1
XM_011531022.1	637	Missense Mutation	CCT,CTT	P141L	XP_011529324.1
XM_011531023.2	637	Missense Mutation	CCT,CTT	P141L	XP_011529325.1
XM_011531024.1	637	Missense Mutation	CCT,CTT	P137L	XP_011529326.1
XM_011531025.1	637	Missense Mutation	CCT,CTT	P141L	XP_011529327.1
XM_011531026.1	637	Missense Mutation	CCT,CTT	P137L	XP_011529328.1
XM_017029803.1	637	Missense Mutation	CCT,CTT	P141L	XP_016885292.1
XM_017029804.1	637	Missense Mutation	CCT,CTT	P137L	XP_016885293.1
XM_017029805.1	637	Missense Mutation	CCT,CTT	P137L	XP_016885294.1
XM_017029806.1	637	Missense Mutation	CCT,CTT	P137L	XP_016885295.1
XM_017029807.1	637	Missense Mutation	CCT,CTT	P137L	XP_016885296.1
XM_017029808.1	637	Missense Mutation	CCT,CTT	P137L	XP_016885297.1
XM_017029809.1	637	Missense Mutation	CCT,CTT	P137L	XP_016885298.1

View Full Product Details