Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGAAGTCCCCTTTGTGCTGTTCCAG[C/G]CACTGGTCCAGCGTCAGGGCCTTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 608382 | ||||||||||||||||||||
Literature Links: |
DNAJA3 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 |
DNAJA3 - DnaJ heat shock protein family (Hsp40) member A3 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
NMRAL1 - NmrA-like family domain containing 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001305141.1 | 1177 | Missense Mutation | TGC,TGG | C,W 288 | NP_001292070.1 | |
NM_001305142.1 | 1177 | Missense Mutation | TGC,TGG | C,W 288 | NP_001292071.1 | |
NM_020677.4 | 1177 | Missense Mutation | TGC,TGG | C,W 288 | NP_065728.1 | |
XM_006720905.3 | 1177 | Missense Mutation | TGC,TGG | C,W 225 | XP_006720968.1 | |
XM_006720906.2 | 1177 | Missense Mutation | TGC,TGG | C,W 224 | XP_006720969.1 | |
XM_011522567.2 | 1177 | Intron | XP_011520869.1 | |||
XM_017023485.1 | 1177 | Missense Mutation | TGC,TGG | C,W 324 | XP_016878974.1 | |
XM_017023486.1 | 1177 | Intron | XP_016878975.1 | |||
XM_017023487.1 | 1177 | Intron | XP_016878976.1 | |||
XM_017023488.1 | 1177 | Intron | XP_016878977.1 | |||
XM_017023489.1 | 1177 | Missense Mutation | TGC,TGG | C,W 224 | XP_016878978.1 | |
XM_017023490.1 | 1177 | Missense Mutation | TGC,TGG | C,W 225 | XP_016878979.1 | |
XM_017023491.1 | 1177 | UTR 3 | XP_016878980.1 | |||
XM_017023492.1 | 1177 | UTR 3 | XP_016878981.1 |