Product Details
- SNP ID
-
rs181643685
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:16897755 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CGGGTCCGGCGCACAGTTCCCGGGC[G/T]AGTGGGCTGTGGGTGCTGACGTTGT
- Phenotype
-
MIM: 608841
MIM: 602779
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
CPAMD8
PubMed Links
Gene Details
- Gene
- CPAMD8
- Gene Name
- C3 and PZP like, alpha-2-macroglobulin domain containing 8
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_015692.2 |
5177 |
Silent Mutation |
CTA,CTC |
L1714L |
NP_056507.2 |
| XM_011527917.1 |
5177 |
Silent Mutation |
CTA,CTC |
L1702L |
XP_011526219.1 |
| XM_011527918.1 |
5177 |
Silent Mutation |
CTA,CTC |
L1714L |
XP_011526220.1 |
| XM_011527919.1 |
5177 |
Silent Mutation |
CTA,CTC |
L1714L |
XP_011526221.1 |
| XM_011527920.2 |
5177 |
Silent Mutation |
CTA,CTC |
L1714L |
XP_011526222.1 |
| XM_011527921.2 |
5177 |
Silent Mutation |
CTA,CTC |
L1714L |
XP_011526223.1 |
| XM_011527922.1 |
5177 |
Silent Mutation |
CTA,CTC |
L1714L |
XP_011526224.1 |
| XM_011527923.1 |
5177 |
Silent Mutation |
CTA,CTC |
L1714L |
XP_011526225.1 |
| XM_011527924.2 |
5177 |
Silent Mutation |
CTA,CTC |
L1714L |
XP_011526226.1 |
| XM_011527925.1 |
5177 |
Silent Mutation |
CTA,CTC |
L971L |
XP_011526227.1 |
| XM_017026594.1 |
5177 |
Silent Mutation |
CTA,CTC |
L1714L |
XP_016882083.1 |
- Gene
- F2RL3
- Gene Name
- F2R like thrombin/trypsin receptor 3
There are no transcripts associated with this gene.
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