Product Details

SNP ID
rs145505544
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:15704102 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCCTCCAGACCTTCTAGAAGGAAC[A/G]AAAGAGGTCTCGTTTCCTCGCCTGT
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 5936 UTR 3 NP_001035202.1
NM_001040114.1 5936 Silent Mutation NP_001035203.1
NM_002474.2 5936 Silent Mutation NP_002465.1
NM_022844.2 5936 UTR 3 NP_074035.1
XM_011522502.2 5936 Intron XP_011520804.1
XM_017023250.1 5936 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 5936 Intron NP_001137451.1
NM_017668.2 5936 Intron NP_060138.1
XM_005255396.4 5936 Intron XP_005255453.1
XM_006720897.3 5936 Intron XP_006720960.1
XM_006720900.3 5936 Intron XP_006720963.1
XM_011522553.2 5936 Intron XP_011520855.1
XM_017023349.1 5936 Intron XP_016878838.1
XM_017023350.1 5936 Intron XP_016878839.1
XM_017023351.1 5936 Intron XP_016878840.1
XM_017023352.1 5936 Intron XP_016878841.1
XM_017023353.1 5936 Intron XP_016878842.1
XM_017023354.1 5936 Intron XP_016878843.1
XM_017023355.1 5936 Intron XP_016878844.1
XM_017023356.1 5936 Intron XP_016878845.1
XM_017023357.1 5936 Intron XP_016878846.1

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