Product Details

SNP ID
rs145788310
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:65596266 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATAACTTAGGGACCCCAGTGTCTT[A/G]GAATTAAATAACAGAGGTAGGGATG
Phenotype
MIM: 309845
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MSN PubMed Links

Gene Details

Gene
MSN
Gene Name
moesin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002444.2 Intron NP_002435.1
XM_005262269.2 Intron XP_005262326.1
XM_011530959.1 Intron XP_011529261.1
XM_017029545.1 Intron XP_016885034.1
XM_017029546.1 Intron XP_016885035.1

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