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Search Thermo Fisher Scientific
CTCACCCACGTCACTGCGCTGACTG[A/C]TACGATCATTGGGCAGGCGTGCACA
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 603727 MIM: 614471 | |||||||||||||||||||||||
Literature Links: |
QARS PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
QARS - glutaminyl-tRNA synthetase | ||||||
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There are no transcripts associated with this gene. |
USP19 - ubiquitin specific peptidase 19 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199160.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1278 | NP_001186089.1 | |
NM_001199161.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1280 | NP_001186090.1 | |
NM_001199162.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1268 | NP_001186091.1 | |
NM_006677.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1177 | NP_006668.1 | |
XM_005264823.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1282 | XP_005264880.1 | |
XM_005264824.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1282 | XP_005264881.1 | |
XM_005264825.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1280 | XP_005264882.1 | |
XM_005264826.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1280 | XP_005264883.1 | |
XM_005264827.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1267 | XP_005264884.1 | |
XM_005264829.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1282 | XP_005264886.1 | |
XM_005264830.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1181 | XP_005264887.1 | |
XM_005264831.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1164 | XP_005264888.1 | |
XM_006712946.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1281 | XP_006713009.1 | |
XM_006712947.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1264 | XP_006713010.1 | |
XM_006712948.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1278 | XP_006713011.1 | |
XM_006712949.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1232 | XP_006713012.1 | |
XM_006712950.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1265 | XP_006713013.1 | |
XM_006712951.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1264 | XP_006713014.1 | |
XM_006712952.2 | 4073 | Missense Mutation | AGC,ATC | S,I 1263 | XP_006713015.1 | |
XM_006712953.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1263 | XP_006713016.1 | |
XM_017005615.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1279 | XP_016861104.1 | |
XM_017005616.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1277 | XP_016861105.1 | |
XM_017005617.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1265 | XP_016861106.1 | |
XM_017005618.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1280 | XP_016861107.1 | |
XM_017005619.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1279 | XP_016861108.1 | |
XM_017005620.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1277 | XP_016861109.1 | |
XM_017005621.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1230 | XP_016861110.1 | |
XM_017005622.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1267 | XP_016861111.1 | |
XM_017005623.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1228 | XP_016861112.1 | |
XM_017005624.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1228 | XP_016861113.1 | |
XM_017005625.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1179 | XP_016861114.1 | |
XM_017005626.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1177 | XP_016861115.1 | |
XM_017005627.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1166 | XP_016861116.1 | |
XM_017005628.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1164 | XP_016861117.1 | |
XM_017005629.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1162 | XP_016861118.1 | |
XM_017005630.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1181 | XP_016861119.1 | |
XM_017005631.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1179 | XP_016861120.1 | |
XM_017005632.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1179 | XP_016861121.1 | |
XM_017005633.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1177 | XP_016861122.1 | |
XM_017005634.1 | 4073 | Missense Mutation | AGC,ATC | S,I 1166 | XP_016861123.1 | |
XM_017005635.1 | 4073 | Missense Mutation | AGC,ATC | S,I 730 | XP_016861124.1 |