Product Details

SNP ID
rs140789717
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:15704024 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCCTTGGTTCCATTGAAGTCTGC[A/G]TCTCGAGTGTCCGTTTCCTCCTCAG
Phenotype
MIM: 160745 MIM: 609449
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MYH11 PubMed Links

Gene Details

Gene
MYH11
Gene Name
myosin heavy chain 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001040113.1 6014 UTR 3 NP_001035202.1
NM_001040114.1 6014 Silent Mutation GAC,GAT D1969D NP_001035203.1
NM_002474.2 6014 Silent Mutation GAC,GAT D1962D NP_002465.1
NM_022844.2 6014 UTR 3 NP_074035.1
XM_011522502.2 6014 Intron XP_011520804.1
XM_017023250.1 6014 Intron XP_016878739.1
Gene
NDE1
Gene Name
nudE neurodevelopment protein 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001143979.1 6014 Intron NP_001137451.1
NM_017668.2 6014 Intron NP_060138.1
XM_005255396.4 6014 Intron XP_005255453.1
XM_006720897.3 6014 Intron XP_006720960.1
XM_006720900.3 6014 Intron XP_006720963.1
XM_011522553.2 6014 Intron XP_011520855.1
XM_017023349.1 6014 Intron XP_016878838.1
XM_017023350.1 6014 Intron XP_016878839.1
XM_017023351.1 6014 Intron XP_016878840.1
XM_017023352.1 6014 Intron XP_016878841.1
XM_017023353.1 6014 Intron XP_016878842.1
XM_017023354.1 6014 Intron XP_016878843.1
XM_017023355.1 6014 Intron XP_016878844.1
XM_017023356.1 6014 Intron XP_016878845.1
XM_017023357.1 6014 Intron XP_016878846.1

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