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SNP ID: rs80292003
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:1473868 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGCTTCAGAAGCATGACCAGTGAGA[A/C]GTCCCTAGGGCCCAGGCCGGGCTAG
Phenotype: MIM: 612034 MIM: 600487
Polymorphism: A/C, Transversion 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	1606	Intron			NP_005874.1
XM_005259475.2	1606	Intron			XP_005259532.1
XM_006722607.2	1606	Intron			XP_006722670.1
XM_006722608.3	1606	Intron			XP_006722671.2
XM_006722609.3	1606	Intron			XP_006722672.1
XM_006722610.3	1606	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	1606	UTR 3			NP_689695.2
XM_005259506.3	1606	UTR 3			XP_005259563.1
XM_006722653.3	1606	UTR 3			XP_006722716.1
XM_017026374.1	1606	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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