Product Details
- SNP ID
-
rs200924494
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.16:15031812 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAAACTGCCAGTGCTGTGCTGTACG[C/T]TCCAGTTGCGTGAAGAGTTCAAGCA
- Phenotype
-
MIM: 615367
MIM: 614244
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
NTAN1
PubMed Links
Gene Details
- Gene
- NTAN1
- Gene Name
- N-terminal asparagine amidase
There are no transcripts associated with this gene.
- Gene
- PDXDC1
- Gene Name
- pyridoxal dependent decarboxylase domain containing 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001285444.1 |
1670 |
Missense Mutation |
CTC,TTC |
L466F |
NP_001272373.1 |
NM_001285445.1 |
1670 |
Missense Mutation |
CTC,TTC |
L465F |
NP_001272374.1 |
NM_001285447.1 |
1670 |
Missense Mutation |
CTC,TTC |
L478F |
NP_001272376.1 |
NM_001285448.1 |
1670 |
Missense Mutation |
CTC,TTC |
L402F |
NP_001272377.1 |
NM_001285449.1 |
1670 |
Intron |
|
|
NP_001272378.1 |
NM_001285450.1 |
1670 |
Intron |
|
|
NP_001272379.1 |
NM_001324019.1 |
1670 |
Missense Mutation |
CTC,TTC |
L492F |
NP_001310948.1 |
NM_001324020.1 |
1670 |
Intron |
|
|
NP_001310949.1 |
NM_001324021.1 |
1670 |
Intron |
|
|
NP_001310950.1 |
NM_015027.3 |
1670 |
Missense Mutation |
CTC,TTC |
L493F |
NP_055842.2 |
XM_005255173.1 |
1670 |
Missense Mutation |
CTC,TTC |
L511F |
XP_005255230.1 |
XM_005255176.2 |
1670 |
Missense Mutation |
CTC,TTC |
L478F |
XP_005255233.1 |
XM_006720865.2 |
1670 |
Missense Mutation |
CTC,TTC |
L451F |
XP_006720928.2 |
XM_017023059.1 |
1670 |
Missense Mutation |
CTC,TTC |
L478F |
XP_016878548.1 |
XM_017023060.1 |
1670 |
Missense Mutation |
CTC,TTC |
L502F |
XP_016878549.1 |
XM_017023061.1 |
1670 |
Missense Mutation |
CTC,TTC |
L478F |
XP_016878550.1 |
XM_017023062.1 |
1670 |
Missense Mutation |
CTC,TTC |
L478F |
XP_016878551.1 |
XM_017023063.1 |
1670 |
Missense Mutation |
CTC,TTC |
L478F |
XP_016878552.1 |
XM_017023064.1 |
1670 |
Missense Mutation |
CTC,TTC |
L451F |
XP_016878553.1 |
XM_017023065.1 |
1670 |
Intron |
|
|
XP_016878554.1 |
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