Product Details

SNP ID
rs112916765
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:77139085 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGGGTAGACAGAAAGAACAATGTG[A/C]ATTTGCATGGGTCTCTCATCTTTAC
Phenotype
MIM: 276903
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
MYO7A PubMed Links

Gene Details

Gene
MYO7A
Gene Name
myosin VIIA
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000260.3 Intron NP_000251.3
NM_001127179.2 Intron NP_001120651.2
NM_001127180.1 Intron NP_001120652.1
XM_011545044.2 Intron XP_011543346.1
XM_011545046.2 Intron XP_011543348.2
XM_011545050.2 Intron XP_011543352.1
XM_017017778.1 Intron XP_016873267.1
XM_017017779.1 Intron XP_016873268.1
XM_017017780.1 Intron XP_016873269.1
XM_017017781.1 Intron XP_016873270.1
XM_017017782.1 Intron XP_016873271.1
XM_017017783.1 Intron XP_016873272.1
XM_017017784.1 Intron XP_016873273.1
XM_017017785.1 Intron XP_016873274.1
XM_017017786.1 Intron XP_016873275.1
XM_017017787.1 Intron XP_016873276.1
XM_017017788.1 Intron XP_016873277.1

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