Product Details

SNP ID

rs200055352

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:10301698 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCTGGACAGCTGCGTGTTGGCCTG[C/T]TCCTCCTGCACAGGAGACAGAGGGG

Phenotype

MIM: 603487

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MYH13 PubMed Links

Gene Details

Gene

MYH13

Gene Name

myosin heavy chain 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003802.2	5763	Silent Mutation	GAA,GAG	E1891E	NP_003793.2

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