Product Details

SNP ID
rs145057132
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:44965709 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGGGGCAGCGGCCACACAAGGTCA[C/T]GCCCGTAGAGTGGCGGCTGCCTTGC
Phenotype
MIM: 600642
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MYO1G PubMed Links

Gene Details

Gene
MYO1G
Gene Name
myosin IG
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_033054.2 2212 Missense Mutation CAT,CGT H770R NP_149043.2
XM_017012503.1 2212 Missense Mutation CAT,CGT H655R XP_016867992.1
XM_017012504.1 2212 Missense Mutation CAT,CGT H532R XP_016867993.1

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