Product Details

SNP ID

rs2302458

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:1467248 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAAAGCAGGCCCCACTCACCACAGC[A/C]AGGTGCCCGTTCTTGGCCTTGGTGA

Phenotype

MIM: 606538

Polymorphism

A/C, Transversion 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	3163	Silent Mutation	CTG,CTT	L1053L	NP_001074248.1
NM_001080950.1	3163	Silent Mutation	CTG,CTT	L1034L	NP_001074419.1
NM_033375.4	3163	Silent Mutation	CTG,CTT	L1018L	NP_203693.3

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