Product Details

SNP ID

rs139266843

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:112520458 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAAGGAATGCAGAAATACTGTGGA[C/T]GTCCATACTTGCAAAGCCCCCAAGA

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	2065	Intron			NP_001295193.1
NM_017744.4	2065	Intron			NP_060214.2
NM_138727.3	2065	Intron			NP_620055.1
NM_138728.2	2065	Intron			NP_620056.1
NM_138729.3	2065	Intron			NP_620057.1
XM_005270963.4	2065	Intron			XP_005271020.1
XM_005270964.3	2065	Intron			XP_005271021.1
XM_011541627.2	2065	Intron			XP_011539929.1
XM_011541628.2	2065	Intron			XP_011539930.1
XM_011541629.2	2065	Intron			XP_011539931.1
XM_011541630.2	2065	Intron			XP_011539932.1
XM_011541631.2	2065	Intron			XP_011539933.1
XM_017001534.1	2065	Intron			XP_016857023.1
XM_017001535.1	2065	Intron			XP_016857024.1
XM_017001536.1	2065	Intron			XP_016857025.1
XM_017001537.1	2065	Intron			XP_016857026.1
XM_017001538.1	2065	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	2065	Silent Mutation	GAC,GAT	D283D	NP_001278809.1
NM_004185.4	2065	Silent Mutation	GAC,GAT	D356D	NP_004176.2
NM_024494.2	2065	Silent Mutation	GAC,GAT	D375D	NP_078613.1

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