Product Details

SNP ID
rs5761163
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:25743411 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTGGGAGCAGAAAAGAGAGGGGTCT[A/G]TATACTCTTAGGCTATGGATGAGTT
Phenotype
MIM: 607295
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MYO18B PubMed Links

Gene Details

Gene
MYO18B
Gene Name
myosin XVIIIB
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318245.1 Intron NP_001305174.1
NM_032608.6 Intron NP_115997.5
XM_011530458.2 Intron XP_011528760.1
XM_011530459.2 Intron XP_011528761.1
XM_011530460.2 Intron XP_011528762.1
XM_011530461.2 Intron XP_011528763.1
XM_011530464.2 Intron XP_011528766.1
XM_011530465.2 Intron XP_011528767.1
XM_011530466.2 Intron XP_011528768.1
XM_017029012.1 Intron XP_016884501.1
XM_017029013.1 Intron XP_016884502.1
XM_017029014.1 Intron XP_016884503.1
XM_017029015.1 Intron XP_016884504.1
XM_017029016.1 Intron XP_016884505.1
XM_017029017.1 Intron XP_016884506.1

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