Product Details

SNP ID
rs77908721
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:80155910 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTCCGGTAATCCCCTGAAGTATC[C/T]CCCTGGCCACAGAAACAAGGAAGAC
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 2017 Silent Mutation GGA,GGG G487G NP_001148.1
NM_001278407.1 2017 Silent Mutation GGA,GGG G487G NP_001265336.1
NM_001278408.1 2017 Silent Mutation GGA,GGG G487G NP_001265337.1
NM_001278409.1 2017 Silent Mutation GGA,GGG G454G NP_001265338.1
NM_145868.1 2017 Silent Mutation GGA,GGG G487G NP_665875.1
NM_145869.1 2017 Silent Mutation GGA,GGG G487G NP_665876.1
XM_005269741.4 2017 Silent Mutation GGA,GGG G587G XP_005269798.1
XM_005269742.1 2017 Intron XP_005269799.1
XM_006717813.1 2017 Intron XP_006717876.1
XM_006717814.3 2017 Intron XP_006717877.1
XM_011539735.1 2017 Intron XP_011538037.1
XM_011539736.2 2017 Intron XP_011538038.1

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