Product Details

SNP ID

rs144361331

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:8475880 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTGTCATCGTCGGAGAGCTCCAGG[A/G]AAGCTCCTTCAAGGTGCAGCTGGCG

Phenotype

MIM: 160776 MIM: 607538

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MYH10 PubMed Links

Gene Details

Gene

MYH10

Gene Name

myosin, heavy chain 10, non-muscle

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256012.1	6102	Missense Mutation	TCC,TTC	S1983F	NP_001242941.1
NM_001256095.1	6102	Missense Mutation	TCC,TTC	S1961F	NP_001243024.1
NM_005964.3	6102	Missense Mutation	TCC,TTC	S1952F	NP_005955.3
XM_011523875.2	6102	Missense Mutation	TCC,TTC	S2013F	XP_011522177.1
XM_011523878.2	6102	Missense Mutation	TCC,TTC	S1992F	XP_011522180.1
XM_011523879.2	6102	Missense Mutation	TCC,TTC	S1991F	XP_011522181.1
XM_011523880.2	6102	Missense Mutation	TCC,TTC	S1982F	XP_011522182.1
XM_017024677.1	6102	Missense Mutation	TCC,TTC	S1962F	XP_016880166.1
XM_017024678.1	6102	Missense Mutation	TCC,TTC	S1962F	XP_016880167.1
XM_017024679.1	6102	Missense Mutation	TCC,TTC	S1962F	XP_016880168.1
XM_017024680.1	6102	Missense Mutation	TCC,TTC	S1961F	XP_016880169.1
XM_017024681.1	6102	Missense Mutation	TCC,TTC	S1952F	XP_016880170.1
XM_017024682.1	6102	Missense Mutation	TCC,TTC	S1952F	XP_016880171.1

Gene

NDEL1

Gene Name

nudE neurodevelopment protein 1 like 1

There are no transcripts associated with this gene.

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