Product Details

SNP ID

rs149845917

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:85255758 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTATAAAAACCGAAGATGATGATGA[G/T]GATGATGTCAAGAGCACTTCTGAAG

Phenotype

MIM: 314990

Polymorphism

G/T, Transversion 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	806	Missense Mutation	GAG,GAT	E193D	NP_068838.3
XM_005262186.2	806	Missense Mutation	GAG,GAT	E193D	XP_005262243.1
XM_005262187.1	806	Missense Mutation	GAG,GAT	E193D	XP_005262244.1
XM_005262188.1	806	Missense Mutation	GAG,GAT	E193D	XP_005262245.1
XM_005262189.2	806	Missense Mutation	GAG,GAT	E193D	XP_005262246.1
XM_011531019.1	806	Missense Mutation	GAG,GAT	E197D	XP_011529321.1
XM_011531020.1	806	Missense Mutation	GAG,GAT	E197D	XP_011529322.1
XM_011531021.1	806	Missense Mutation	GAG,GAT	E197D	XP_011529323.1
XM_011531022.1	806	Missense Mutation	GAG,GAT	E197D	XP_011529324.1
XM_011531023.2	806	Missense Mutation	GAG,GAT	E197D	XP_011529325.1
XM_011531024.1	806	Missense Mutation	GAG,GAT	E193D	XP_011529326.1
XM_011531025.1	806	Missense Mutation	GAG,GAT	E197D	XP_011529327.1
XM_011531026.1	806	Missense Mutation	GAG,GAT	E193D	XP_011529328.1
XM_017029803.1	806	Missense Mutation	GAG,GAT	E197D	XP_016885292.1
XM_017029804.1	806	Missense Mutation	GAG,GAT	E193D	XP_016885293.1
XM_017029805.1	806	Missense Mutation	GAG,GAT	E193D	XP_016885294.1
XM_017029806.1	806	Missense Mutation	GAG,GAT	E193D	XP_016885295.1
XM_017029807.1	806	Missense Mutation	GAG,GAT	E193D	XP_016885296.1
XM_017029808.1	806	Missense Mutation	GAG,GAT	E193D	XP_016885297.1
XM_017029809.1	806	Missense Mutation	GAG,GAT	E193D	XP_016885298.1

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