Product Details
- SNP ID
-
rs142037382
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:49109036 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCACCAAAGCCGCCACGGTGCCCAG[C/G]ACAAAGTACCGGAGGCAGCCCTCAT
- Phenotype
-
MIM: 603727
MIM: 614471
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
MIR6890
PubMed Links
Gene Details
- Gene
- MIR6890
- Gene Name
- microRNA 6890
There are no transcripts associated with this gene.
- Gene
- QARS
- Gene Name
- glutaminyl-tRNA synthetase
There are no transcripts associated with this gene.
- Gene
- USP19
- Gene Name
- ubiquitin specific peptidase 19
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001199160.1 |
4422 |
Silent Mutation |
GTC,GTG |
V1394V |
NP_001186089.1 |
| NM_001199161.1 |
4422 |
Intron |
|
|
NP_001186090.1 |
| NM_001199162.1 |
4422 |
Intron |
|
|
NP_001186091.1 |
| NM_006677.2 |
4422 |
Silent Mutation |
GTC,GTG |
V1293V |
NP_006668.1 |
| XM_005264823.2 |
4422 |
Silent Mutation |
GTC,GTG |
V1398V |
XP_005264880.1 |
| XM_005264824.2 |
4422 |
Silent Mutation |
GTC,GTG |
V1398V |
XP_005264881.1 |
| XM_005264825.2 |
4422 |
Silent Mutation |
GTC,GTG |
V1396V |
XP_005264882.1 |
| XM_005264826.2 |
4422 |
Silent Mutation |
GTC,GTG |
V1396V |
XP_005264883.1 |
| XM_005264827.2 |
4422 |
Silent Mutation |
GTC,GTG |
V1383V |
XP_005264884.1 |
| XM_005264829.2 |
4422 |
Intron |
|
|
XP_005264886.1 |
| XM_005264830.2 |
4422 |
Silent Mutation |
GTC,GTG |
V1297V |
XP_005264887.1 |
| XM_005264831.2 |
4422 |
Intron |
|
|
XP_005264888.1 |
| XM_006712946.2 |
4422 |
Silent Mutation |
GTC,GTG |
V1397V |
XP_006713009.1 |
| XM_006712947.2 |
4422 |
Silent Mutation |
GTC,GTG |
V1380V |
XP_006713010.1 |
| XM_006712948.2 |
4422 |
Intron |
|
|
XP_006713011.1 |
| XM_006712949.2 |
4422 |
Silent Mutation |
GTC,GTG |
V1348V |
XP_006713012.1 |
| XM_006712950.2 |
4422 |
Intron |
|
|
XP_006713013.1 |
| XM_006712951.2 |
4422 |
Intron |
|
|
XP_006713014.1 |
| XM_006712952.2 |
4422 |
Intron |
|
|
XP_006713015.1 |
| XM_006712953.1 |
4422 |
Silent Mutation |
GTC,GTG |
V1379V |
XP_006713016.1 |
| XM_017005615.1 |
4422 |
Silent Mutation |
GTC,GTG |
V1395V |
XP_016861104.1 |
| XM_017005616.1 |
4422 |
Silent Mutation |
GTC,GTG |
V1393V |
XP_016861105.1 |
| XM_017005617.1 |
4422 |
Silent Mutation |
GTC,GTG |
V1381V |
XP_016861106.1 |
| XM_017005618.1 |
4422 |
Intron |
|
|
XP_016861107.1 |
| XM_017005619.1 |
4422 |
Intron |
|
|
XP_016861108.1 |
| XM_017005620.1 |
4422 |
Intron |
|
|
XP_016861109.1 |
| XM_017005621.1 |
4422 |
Silent Mutation |
GTC,GTG |
V1346V |
XP_016861110.1 |
| XM_017005622.1 |
4422 |
Intron |
|
|
XP_016861111.1 |
| XM_017005623.1 |
4422 |
Silent Mutation |
GTC,GTG |
V1344V |
XP_016861112.1 |
| XM_017005624.1 |
4422 |
Intron |
|
|
XP_016861113.1 |
| XM_017005625.1 |
4422 |
Silent Mutation |
GTC,GTG |
V1295V |
XP_016861114.1 |
| XM_017005626.1 |
4422 |
Silent Mutation |
GTC,GTG |
V1293V |
XP_016861115.1 |
| XM_017005627.1 |
4422 |
Silent Mutation |
GTC,GTG |
V1282V |
XP_016861116.1 |
| XM_017005628.1 |
4422 |
Silent Mutation |
GTC,GTG |
V1280V |
XP_016861117.1 |
| XM_017005629.1 |
4422 |
Silent Mutation |
GTC,GTG |
V1278V |
XP_016861118.1 |
| XM_017005630.1 |
4422 |
Intron |
|
|
XP_016861119.1 |
| XM_017005631.1 |
4422 |
Intron |
|
|
XP_016861120.1 |
| XM_017005632.1 |
4422 |
Intron |
|
|
XP_016861121.1 |
| XM_017005633.1 |
4422 |
Intron |
|
|
XP_016861122.1 |
| XM_017005634.1 |
4422 |
Intron |
|
|
XP_016861123.1 |
| XM_017005635.1 |
4422 |
Silent Mutation |
GTC,GTG |
V846V |
XP_016861124.1 |
View Full Product Details