Product Details
- SNP ID
-
rs138582821
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
9
- Location
-
Chr.1:242089974 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGGTTGGCTGTAAGGTTTTGGCATA[C/T]GGTGAATACCAGTCCCTTTCAAACA
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
PLD5
PubMed Links
Gene Details
- Gene
- PLD5
- Gene Name
- phospholipase D family member 5
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001195811.1 |
1718 |
Silent Mutation |
CCA,CCG |
P435P |
NP_001182740.1 |
NM_001195812.1 |
1718 |
Silent Mutation |
CCA,CCG |
P289P |
NP_001182741.1 |
NM_001320272.1 |
1718 |
Silent Mutation |
CCA,CCG |
P405P |
NP_001307201.1 |
NM_152666.2 |
1718 |
Silent Mutation |
CCA,CCG |
P497P |
NP_689879.2 |
XM_006711752.2 |
1718 |
Silent Mutation |
CCA,CCG |
P497P |
XP_006711815.1 |
XM_011544115.2 |
1718 |
Silent Mutation |
CCA,CCG |
P406P |
XP_011542417.1 |
XM_011544116.2 |
1718 |
Silent Mutation |
CCA,CCG |
P406P |
XP_011542418.1 |
XM_011544119.2 |
1718 |
Silent Mutation |
CCA,CCG |
P362P |
XP_011542421.2 |
XM_011544120.2 |
1718 |
Silent Mutation |
CCA,CCG |
P289P |
XP_011542422.1 |
XM_011544121.2 |
1718 |
Silent Mutation |
CCA,CCG |
P289P |
XP_011542423.1 |
XM_011544122.2 |
1718 |
Silent Mutation |
CCA,CCG |
P289P |
XP_011542424.1 |
XM_017000567.1 |
1718 |
Silent Mutation |
CCA,CCG |
P405P |
XP_016856056.1 |
XM_017000568.1 |
1718 |
Silent Mutation |
CCA,CCG |
P405P |
XP_016856057.1 |
XM_017000569.1 |
1718 |
Silent Mutation |
CCA,CCG |
P289P |
XP_016856058.1 |
XM_017000570.1 |
1718 |
Silent Mutation |
CCA,CCG |
P289P |
XP_016856059.1 |
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