Product Details

SNP ID

rs142956872

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:80157706 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACTCTGATCTGATGTCCAGGAGGT[C/T]GGTCTCGCTGCGAGACACCATGATG

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	1949	Missense Mutation	AAC,GAC	N465D	NP_001148.1
NM_001278407.1	1949	Missense Mutation	AAC,GAC	N465D	NP_001265336.1
NM_001278408.1	1949	Missense Mutation	AAC,GAC	N465D	NP_001265337.1
NM_001278409.1	1949	Missense Mutation	AAC,GAC	N432D	NP_001265338.1
NM_145868.1	1949	Missense Mutation	AAC,GAC	N465D	NP_665875.1
NM_145869.1	1949	Missense Mutation	AAC,GAC	N465D	NP_665876.1
XM_005269741.4	1949	Missense Mutation	AAC,GAC	N565D	XP_005269798.1
XM_005269742.1	1949	Missense Mutation	AAC,GAC	N465D	XP_005269799.1
XM_006717813.1	1949	Missense Mutation	AAC,GAC	N465D	XP_006717876.1
XM_006717814.3	1949	Missense Mutation	AAC,GAC	N465D	XP_006717877.1
XM_011539735.1	1949	Missense Mutation	AAC,GAC	N465D	XP_011538037.1
XM_011539736.2	1949	Intron			XP_011538038.1

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