Product Details

SNP ID
rs146413415
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:15704023 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGGCCTTGGTTCCATTGAAGTCTG[C/T]GTCTCGAGTGTCCGTTTCCTCCTCA
Phenotype
MIM: 160745 MIM: 609449
Polymorphism
C/T, 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 6015 UTR 3 NP_001035202.1
NM_001040114.1 6015 Missense Mutation ACA,GCA T1970A NP_001035203.1
NM_002474.2 6015 Missense Mutation ACA,GCA T1963A NP_002465.1
NM_022844.2 6015 UTR 3 NP_074035.1
XM_011522502.2 6015 Intron XP_011520804.1
XM_017023250.1 6015 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 6015 Intron NP_001137451.1
NM_017668.2 6015 Intron NP_060138.1
XM_005255396.4 6015 Intron XP_005255453.1
XM_006720897.3 6015 Intron XP_006720960.1
XM_006720900.3 6015 Intron XP_006720963.1
XM_011522553.2 6015 Intron XP_011520855.1
XM_017023349.1 6015 Intron XP_016878838.1
XM_017023350.1 6015 Intron XP_016878839.1
XM_017023351.1 6015 Intron XP_016878840.1
XM_017023352.1 6015 Intron XP_016878841.1
XM_017023353.1 6015 Intron XP_016878842.1
XM_017023354.1 6015 Intron XP_016878843.1
XM_017023355.1 6015 Intron XP_016878844.1
XM_017023356.1 6015 Intron XP_016878845.1
XM_017023357.1 6015 Intron XP_016878846.1

View Full Product Details