Product Details

SNP ID

rs201365950

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:1468028 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATCAATCCTCTGCTTGACTTTGGC[A/G]TCCTCCACGATGACGACGGCGTTGG

Phenotype

MIM: 606538

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MYO1C PubMed Links

Gene Details

Gene

MYO1C

Gene Name

myosin IC

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080779.1	2860	Silent Mutation			NP_001074248.1
NM_001080950.1	2860	Silent Mutation			NP_001074419.1
NM_033375.4	2860	Silent Mutation			NP_203693.3

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