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GTTGTTCAGAGCAGGTCAGGCAGGA[C/T]GAGGCCAGGAGGCTTTGGTTCGACA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606618 MIM: 607291 | ||||||||||||||||||||
Literature Links: |
DUSP14 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | 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 |
DUSP14 - dual specificity phosphatase 14 | ||||||
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There are no transcripts associated with this gene. |
SYNRG - synergin, gamma | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001163544.2 | 4132 | Missense Mutation | ATC,GTC | I,V 1231 | NP_001157016.1 | |
NM_001163545.2 | 4132 | Missense Mutation | ATC,GTC | I,V 1230 | NP_001157017.1 | |
NM_001163546.2 | 4132 | Missense Mutation | ATC,GTC | I,V 1174 | NP_001157018.1 | |
NM_001163547.2 | 4132 | Missense Mutation | ATC,GTC | I,V 1103 | NP_001157019.1 | |
NM_007247.5 | 4132 | Missense Mutation | ATC,GTC | I,V 1309 | NP_009178.3 | |
NM_080550.4 | 4132 | Missense Mutation | ATC,GTC | I,V 1219 | NP_542117.3 | |
NM_198882.2 | 4132 | Missense Mutation | ATC,GTC | I,V 1254 | NP_942583.1 | |
XM_005256980.4 | 4132 | Missense Mutation | ATC,GTC | I,V 1410 | XP_005257037.1 | |
XM_017024076.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1433 | XP_016879565.1 | |
XM_017024077.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1432 | XP_016879566.1 | |
XM_017024078.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1421 | XP_016879567.1 | |
XM_017024079.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1412 | XP_016879568.1 | |
XM_017024080.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1406 | XP_016879569.1 | |
XM_017024081.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1405 | XP_016879570.1 | |
XM_017024082.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1398 | XP_016879571.1 | |
XM_017024083.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1388 | XP_016879572.1 | |
XM_017024084.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1387 | XP_016879573.1 | |
XM_017024085.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1377 | XP_016879574.1 | |
XM_017024086.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1365 | XP_016879575.1 | |
XM_017024087.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1364 | XP_016879576.1 | |
XM_017024088.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1355 | XP_016879577.1 | |
XM_017024089.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1353 | XP_016879578.1 | |
XM_017024090.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1332 | XP_016879579.1 | |
XM_017024091.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1331 | XP_016879580.1 | |
XM_017024092.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1331 | XP_016879581.1 | |
XM_017024093.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1297 | XP_016879582.1 | |
XM_017024094.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1296 | XP_016879583.1 | |
XM_017024095.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1288 | XP_016879584.1 | |
XM_017024096.1 | 4132 | Intron | XP_016879585.1 | |||
XM_017024097.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1264 | XP_016879586.1 | |
XM_017024098.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1263 | XP_016879587.1 | |
XM_017024099.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1253 | XP_016879588.1 | |
XM_017024100.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1251 | XP_016879589.1 | |
XM_017024101.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1250 | XP_016879590.1 | |
XM_017024102.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1218 | XP_016879591.1 | |
XM_017024103.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1208 | XP_016879592.1 | |
XM_017024104.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1185 | XP_016879593.1 | |
XM_017024105.1 | 4132 | Intron | XP_016879594.1 | |||
XM_017024106.1 | 4132 | Missense Mutation | ATC,GTC | I,V 1186 | XP_016879595.1 |