Product Details

SNP ID

rs143447584

Assay Type

Functionally tested

NCBI dbSNP Submissions

6

Location

Chr.1:243271001 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTTAATCAGCTCAAAGATTTGTTG[C/T]GCCAACAAGCAGATAAGGAAAGTGA

Phenotype

MIM: 613524

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SDCCAG8 PubMed Links

Gene Details

Gene

SDCCAG8

Gene Name

serologically defined colon cancer antigen 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006642.3	381	Missense Mutation	CGC,TGC	R82C	NP_006633.1
XM_005273013.4	381	Missense Mutation	CGC,TGC	R82C	XP_005273070.1
XM_005273018.1	381	UTR 5			XP_005273075.1
XM_005273021.4	381	UTR 5			XP_005273078.1
XM_005273022.3	381	UTR 5			XP_005273079.1
XM_005273023.4	381	Missense Mutation	CGC,TGC	R82C	XP_005273080.1
XM_006711727.3	381	Missense Mutation	CGC,TGC	R92C	XP_006711790.1
XM_006711728.3	381	Missense Mutation	CGC,TGC	R92C	XP_006711791.1
XM_011544021.2	381	Missense Mutation	CGC,TGC	R92C	XP_011542323.1
XM_011544022.2	381	Missense Mutation	CGC,TGC	R82C	XP_011542324.1
XM_011544023.2	381	Missense Mutation	CGC,TGC	R92C	XP_011542325.1
XM_011544024.2	381	Missense Mutation	CGC,TGC	R92C	XP_011542326.1
XM_011544026.2	381	Missense Mutation	CGC,TGC	R92C	XP_011542328.1
XM_011544028.2	381	Missense Mutation	CGC,TGC	R92C	XP_011542330.1
XM_011544029.2	381	Missense Mutation	CGC,TGC	R92C	XP_011542331.1
XM_011544030.2	381	Intron			XP_011542332.1
XM_017000103.1	381	Missense Mutation	CGC,TGC	R92C	XP_016855592.1
XM_017000104.1	381	Missense Mutation	CGC,TGC	R82C	XP_016855593.1
XM_017000105.1	381	Missense Mutation	CGC,TGC	R82C	XP_016855594.1
XM_017000106.1	381	UTR 5			XP_016855595.1
XM_017000107.1	381	UTR 5			XP_016855596.1
XM_017000108.1	381	UTR 5			XP_016855597.1
XM_017000109.1	381	Missense Mutation	CGC,TGC	R92C	XP_016855598.1

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