Product Details

SNP ID

rs11878689

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:1473345 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCTGAGACCCCCCAGGTTAGATCCC[C/T]GGAAGCAGAGCCAGAAAGCAGAAAC

Phenotype

MIM: 612034 MIM: 600487

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

APC2 PubMed Links

Gene Details

Gene

APC2

Gene Name

APC2, WNT signaling pathway regulator

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005883.2	2129	Intron			NP_005874.1
XM_005259475.2	2129	Intron			XP_005259532.1
XM_006722607.2	2129	Intron			XP_006722670.1
XM_006722608.3	2129	Intron			XP_006722671.2
XM_006722609.3	2129	Intron			XP_006722672.1
XM_006722610.3	2129	Intron			XP_006722673.2

Gene

C19orf25

Gene Name

chromosome 19 open reading frame 25

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152482.2	2129	UTR 3			NP_689695.2
XM_005259506.3	2129	UTR 3			XP_005259563.1
XM_006722653.3	2129	UTR 3			XP_006722716.1
XM_017026374.1	2129	UTR 3			XP_016881863.1

Gene

PCSK4

Gene Name

proprotein convertase subtilisin/kexin type 4

There are no transcripts associated with this gene.

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