Product Details
- SNP ID
-
rs61748720
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:37519041 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGATACTGGTGCCCTCCATAGGCCA[A/G]CTTGAAACTGTCTGTTTCTGAGTTG
- Phenotype
-
MIM: 606618
MIM: 607291
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
DUSP14
PubMed Links
Gene Details
- Gene
- DUSP14
- Gene Name
- dual specificity phosphatase 14
There are no transcripts associated with this gene.
- Gene
- SYNRG
- Gene Name
- synergin, gamma
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001163544.2 |
4051 |
Silent Mutation |
CTG,TTG |
L1204L |
NP_001157016.1 |
| NM_001163545.2 |
4051 |
Silent Mutation |
CTG,TTG |
L1203L |
NP_001157017.1 |
| NM_001163546.2 |
4051 |
Silent Mutation |
CTG,TTG |
L1147L |
NP_001157018.1 |
| NM_001163547.2 |
4051 |
Silent Mutation |
CTG,TTG |
L1076L |
NP_001157019.1 |
| NM_007247.5 |
4051 |
Silent Mutation |
CTG,TTG |
L1282L |
NP_009178.3 |
| NM_080550.4 |
4051 |
Silent Mutation |
CTG,TTG |
L1192L |
NP_542117.3 |
| NM_198882.2 |
4051 |
Silent Mutation |
CTG,TTG |
L1227L |
NP_942583.1 |
| XM_005256980.4 |
4051 |
Silent Mutation |
CTG,TTG |
L1383L |
XP_005257037.1 |
| XM_017024076.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1406L |
XP_016879565.1 |
| XM_017024077.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1405L |
XP_016879566.1 |
| XM_017024078.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1394L |
XP_016879567.1 |
| XM_017024079.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1385L |
XP_016879568.1 |
| XM_017024080.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1379L |
XP_016879569.1 |
| XM_017024081.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1378L |
XP_016879570.1 |
| XM_017024082.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1371L |
XP_016879571.1 |
| XM_017024083.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1361L |
XP_016879572.1 |
| XM_017024084.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1360L |
XP_016879573.1 |
| XM_017024085.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1350L |
XP_016879574.1 |
| XM_017024086.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1338L |
XP_016879575.1 |
| XM_017024087.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1337L |
XP_016879576.1 |
| XM_017024088.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1328L |
XP_016879577.1 |
| XM_017024089.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1326L |
XP_016879578.1 |
| XM_017024090.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1305L |
XP_016879579.1 |
| XM_017024091.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1304L |
XP_016879580.1 |
| XM_017024092.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1304L |
XP_016879581.1 |
| XM_017024093.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1270L |
XP_016879582.1 |
| XM_017024094.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1269L |
XP_016879583.1 |
| XM_017024095.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1261L |
XP_016879584.1 |
| XM_017024096.1 |
4051 |
Intron |
|
|
XP_016879585.1 |
| XM_017024097.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1237L |
XP_016879586.1 |
| XM_017024098.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1236L |
XP_016879587.1 |
| XM_017024099.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1226L |
XP_016879588.1 |
| XM_017024100.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1224L |
XP_016879589.1 |
| XM_017024101.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1223L |
XP_016879590.1 |
| XM_017024102.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1191L |
XP_016879591.1 |
| XM_017024103.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1181L |
XP_016879592.1 |
| XM_017024104.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1158L |
XP_016879593.1 |
| XM_017024105.1 |
4051 |
Intron |
|
|
XP_016879594.1 |
| XM_017024106.1 |
4051 |
Silent Mutation |
CTG,TTG |
L1159L |
XP_016879595.1 |
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