Product Details

SNP ID

rs201450866

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:1481879 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGGACGGGGCCTCCGAGGGTCAC[A/G]GCCAGGAGGCTCAGCACCATGGCCG

Phenotype

MIM: 612034 MIM: 600487 MIM: 609346

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

APC2 PubMed Links

Gene Details

Gene

APC2

Gene Name

APC2, WNT signaling pathway regulator

There are no transcripts associated with this gene.

Gene

C19orf25

Gene Name

chromosome 19 open reading frame 25

There are no transcripts associated with this gene.

Gene

PCSK4

Gene Name

proprotein convertase subtilisin/kexin type 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017573.4	1812	Silent Mutation	GCC,GCT	A716A	NP_060043.2
XM_005259586.1	1812	Silent Mutation	GCC,GCT	A528A	XP_005259643.1
XM_011528085.2	1812	Silent Mutation	GCC,GCT	A743A	XP_011526387.1
XM_011528086.2	1812	Silent Mutation	GCC,GCT	A734A	XP_011526388.1
XM_011528087.2	1812	Silent Mutation	GCC,GCT	A685A	XP_011526389.1
XM_011528088.2	1812	Silent Mutation	GCC,GCT	A681A	XP_011526390.1
XM_011528089.2	1812	Silent Mutation	GCC,GCT	A649A	XP_011526391.1
XM_011528090.2	1812	Silent Mutation	GCC,GCT	A622A	XP_011526392.1
XM_011528091.2	1812	Silent Mutation	GCC,GCT	A619A	XP_011526393.1
XM_011528092.2	1812	Intron			XP_011526394.1
XM_011528093.2	1812	UTR 3			XP_011526395.1
XM_011528094.1	1812	Silent Mutation	GCC,GCT	A528A	XP_011526396.1
XM_011528095.2	1812	Intron			XP_011526397.1
XM_011528096.1	1812	Silent Mutation	GCC,GCT	A494A	XP_011526398.1
XM_017026897.1	1812	Intron			XP_016882386.1

Gene

REEP6

Gene Name

receptor accessory protein 6

There are no transcripts associated with this gene.

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