Product Details

SNP ID

rs1802932

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:80157730 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCGGTCTCGCTGCGAGACACCATGA[C/T]GCGAATCAGGGTCCGGTCCTTTGTT

Phenotype

MIM: 602572

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ANXA11 PubMed Links

Gene Details

Gene

ANXA11

Gene Name

annexin A11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001157.2	1925	Missense Mutation	ATC,GTC	I457V	NP_001148.1
NM_001278407.1	1925	Missense Mutation	ATC,GTC	I457V	NP_001265336.1
NM_001278408.1	1925	Missense Mutation	ATC,GTC	I457V	NP_001265337.1
NM_001278409.1	1925	Missense Mutation	ATC,GTC	I424V	NP_001265338.1
NM_145868.1	1925	Missense Mutation	ATC,GTC	I457V	NP_665875.1
NM_145869.1	1925	Missense Mutation	ATC,GTC	I457V	NP_665876.1
XM_005269741.4	1925	Missense Mutation	ATC,GTC	I557V	XP_005269798.1
XM_005269742.1	1925	Missense Mutation	ATC,GTC	I457V	XP_005269799.1
XM_006717813.1	1925	Missense Mutation	ATC,GTC	I457V	XP_006717876.1
XM_006717814.3	1925	Missense Mutation	ATC,GTC	I457V	XP_006717877.1
XM_011539735.1	1925	Missense Mutation	ATC,GTC	I457V	XP_011538037.1
XM_011539736.2	1925	Intron			XP_011538038.1

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