Product Details
- SNP ID
-
rs201726139
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:21421402 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCTGCTAGAGGATTTGGTAGAATTC[G/T]TGGAGCCAATGGCTTTGAAGGTTCT
- Phenotype
-
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
ZNF385D
PubMed Links
Gene Details
- Gene
- ZNF385D
- Gene Name
- zinc finger protein 385D
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_024697.2 |
1612 |
Silent Mutation |
AGA,CGA |
R334R |
NP_078973.1 |
| XM_011534122.1 |
1612 |
Intron |
|
|
XP_011532424.1 |
| XM_011534123.2 |
1612 |
Intron |
|
|
XP_011532425.1 |
| XM_011534124.2 |
1612 |
Intron |
|
|
XP_011532426.1 |
| XM_017007191.1 |
1612 |
Silent Mutation |
AGA,CGA |
R454R |
XP_016862680.1 |
| XM_017007192.1 |
1612 |
Silent Mutation |
AGA,CGA |
R435R |
XP_016862681.1 |
| XM_017007193.1 |
1612 |
Silent Mutation |
AGA,CGA |
R383R |
XP_016862682.1 |
| XM_017007194.1 |
1612 |
Silent Mutation |
AGA,CGA |
R370R |
XP_016862683.1 |
| XM_017007195.1 |
1612 |
Silent Mutation |
AGA,CGA |
R368R |
XP_016862684.1 |
| XM_017007196.1 |
1612 |
Silent Mutation |
AGA,CGA |
R353R |
XP_016862685.1 |
| XM_017007197.1 |
1612 |
Silent Mutation |
AGA,CGA |
R350R |
XP_016862686.1 |
| XM_017007198.1 |
1612 |
Silent Mutation |
AGA,CGA |
R349R |
XP_016862687.1 |
| XM_017007199.1 |
1612 |
Silent Mutation |
AGA,CGA |
R301R |
XP_016862688.1 |
| XM_017007200.1 |
1612 |
Silent Mutation |
AGA,CGA |
R298R |
XP_016862689.1 |
| XM_017007201.1 |
1612 |
Silent Mutation |
AGA,CGA |
R240R |
XP_016862690.1 |
| XM_017007202.1 |
1612 |
Silent Mutation |
AGA,CGA |
R201R |
XP_016862691.1 |
| XM_017007203.1 |
1612 |
Intron |
|
|
XP_016862692.1 |
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