Product Details

SNP ID
rs201872478
Assay Type
Functionally tested
NCBI dbSNP Submissions
2
Location
Chr.1:112520370 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGTGCTGTGGCCGAGGGTACGACA[C/T]AACTCGAGTCACCCGTGTTACCCAG
Phenotype
MIM: 601968
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ST7L PubMed Links

Gene Details

Gene
ST7L
Gene Name
suppression of tumorigenicity 7 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001308264.1 1977 Intron NP_001295193.1
NM_017744.4 1977 Intron NP_060214.2
NM_138727.3 1977 Intron NP_620055.1
NM_138728.2 1977 Intron NP_620056.1
NM_138729.3 1977 Intron NP_620057.1
XM_005270963.4 1977 Intron XP_005271020.1
XM_005270964.3 1977 Intron XP_005271021.1
XM_011541627.2 1977 Intron XP_011539929.1
XM_011541628.2 1977 Intron XP_011539930.1
XM_011541629.2 1977 Intron XP_011539931.1
XM_011541630.2 1977 Intron XP_011539932.1
XM_011541631.2 1977 Intron XP_011539933.1
XM_017001534.1 1977 Intron XP_016857023.1
XM_017001535.1 1977 Intron XP_016857024.1
XM_017001536.1 1977 Intron XP_016857025.1
XM_017001537.1 1977 Intron XP_016857026.1
XM_017001538.1 1977 Intron XP_016857027.1
Gene
WNT2B
Gene Name
Wnt family member 2B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001291880.1 1977 Missense Mutation ACA,ATA T254I NP_001278809.1
NM_004185.4 1977 Missense Mutation ACA,ATA T327I NP_004176.2
NM_024494.2 1977 Missense Mutation ACA,ATA T346I NP_078613.1

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