Product Details

SNP ID
rs1875184
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:15703986 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTGCCGTGGTGCAAAACTGTAGAAA[C/G]TTGCTTATTCACTGGCCTTGGTTCC
Phenotype
MIM: 160745 MIM: 609449
Polymorphism
C/G, Transversion 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 6052 UTR 3 NP_001035202.1
NM_001040114.1 6052 UTR 3 NP_001035203.1
NM_002474.2 6052 UTR 3 NP_002465.1
NM_022844.2 6052 UTR 3 NP_074035.1
XM_011522502.2 6052 Intron XP_011520804.1
XM_017023250.1 6052 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 6052 Intron NP_001137451.1
NM_017668.2 6052 Intron NP_060138.1
XM_005255396.4 6052 Intron XP_005255453.1
XM_006720897.3 6052 Intron XP_006720960.1
XM_006720900.3 6052 Intron XP_006720963.1
XM_011522553.2 6052 Intron XP_011520855.1
XM_017023349.1 6052 Intron XP_016878838.1
XM_017023350.1 6052 Intron XP_016878839.1
XM_017023351.1 6052 Intron XP_016878840.1
XM_017023352.1 6052 Intron XP_016878841.1
XM_017023353.1 6052 Intron XP_016878842.1
XM_017023354.1 6052 Intron XP_016878843.1
XM_017023355.1 6052 Intron XP_016878844.1
XM_017023356.1 6052 Intron XP_016878845.1
XM_017023357.1 6052 Intron XP_016878846.1

View Full Product Details