Product Details

SNP ID
rs11611277
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:109388829 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCGACAACCTCCGCAAGCGTTTCAG[A/C]GAGAACCTCATATACGTAACGTGAC
Phenotype
MIM: 614636
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
MYO1H PubMed Links

Gene Details

Gene
MYO1H
Gene Name
myosin IH
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001101421.3 553 Silent Mutation AGA,AGC R37S NP_001094891.3
XM_011538223.2 553 Missense Mutation AGA,AGC R37S XP_011536525.1
XM_017019207.1 553 Missense Mutation AGA,AGC R37S XP_016874696.1

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