Product Details
- SNP ID
-
rs150984670
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:1481870 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACATGCCGCAGAGGACGGGGCCTCC[A/G]AGGGTCACGGCCAGGAGGCTCAGCA
- 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 |
1821 |
Silent Mutation |
CTC,CTT |
L719L |
NP_060043.2 |
XM_005259586.1 |
1821 |
Silent Mutation |
CTC,CTT |
L531L |
XP_005259643.1 |
XM_011528085.2 |
1821 |
Silent Mutation |
CTC,CTT |
L746L |
XP_011526387.1 |
XM_011528086.2 |
1821 |
Silent Mutation |
CTC,CTT |
L737L |
XP_011526388.1 |
XM_011528087.2 |
1821 |
Silent Mutation |
CTC,CTT |
L688L |
XP_011526389.1 |
XM_011528088.2 |
1821 |
Silent Mutation |
CTC,CTT |
L684L |
XP_011526390.1 |
XM_011528089.2 |
1821 |
Silent Mutation |
CTC,CTT |
L652L |
XP_011526391.1 |
XM_011528090.2 |
1821 |
Silent Mutation |
CTC,CTT |
L625L |
XP_011526392.1 |
XM_011528091.2 |
1821 |
Silent Mutation |
CTC,CTT |
L622L |
XP_011526393.1 |
XM_011528092.2 |
1821 |
Intron |
|
|
XP_011526394.1 |
XM_011528093.2 |
1821 |
UTR 3 |
|
|
XP_011526395.1 |
XM_011528094.1 |
1821 |
Silent Mutation |
CTC,CTT |
L531L |
XP_011526396.1 |
XM_011528095.2 |
1821 |
Intron |
|
|
XP_011526397.1 |
XM_011528096.1 |
1821 |
Silent Mutation |
CTC,CTT |
L497L |
XP_011526398.1 |
XM_017026897.1 |
1821 |
Intron |
|
|
XP_016882386.1 |
- Gene
- REEP6
- Gene Name
- receptor accessory protein 6
There are no transcripts associated with this gene.
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