Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGATATAAGGAATAAGGAGGATTA[A/G]AGACCATCAACTGGCTTAATAATGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
DNAJB14 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
DNAJB14 - DnaJ heat shock protein family (Hsp40) member B14 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031723.3 | 1351 | Missense Mutation | TCT,TTT | S,F 271 | NP_001026893.1 | |
NM_001278310.1 | 1351 | Missense Mutation | TCT,TTT | S,F 204 | NP_001265239.1 | |
NM_001278311.1 | 1351 | Intron | NP_001265240.1 | |||
XM_011532262.2 | 1351 | Missense Mutation | TCT,TTT | S,F 186 | XP_011530564.1 | |
XM_011532263.2 | 1351 | Missense Mutation | TCT,TTT | S,F 186 | XP_011530565.1 | |
XM_011532265.2 | 1351 | Missense Mutation | TCT,TTT | S,F 183 | XP_011530567.1 | |
XM_017008628.1 | 1351 | Missense Mutation | TCT,TTT | S,F 183 | XP_016864117.1 |