Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGACGCTGGTGGGTACCACCTGAC[A/G]ACGAAGACTGTGTGTCTGAGAAGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 603892 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
EFTUD2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
EFTUD2 - elongation factor Tu GTP binding domain containing 2 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
HIGD1B - HIG1 hypoxia inducible domain family member 1B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271880.1 | 182 | Missense Mutation | AAC,GAC | N,D 13 | NP_001258809.1 | |
NM_016438.3 | 182 | Missense Mutation | AAC,GAC | N,D 13 | NP_057522.1 | |
XM_006721946.2 | 182 | Missense Mutation | AAC,GAC | N,D 13 | XP_006722009.1 | |
XM_006721947.3 | 182 | Missense Mutation | AAC,GAC | N,D 13 | XP_006722010.1 | |
XM_006721948.3 | 182 | Missense Mutation | AAC,GAC | N,D 13 | XP_006722011.1 | |
XM_011524891.2 | 182 | Missense Mutation | AAC,GAC | N,D 13 | XP_011523193.1 | |
XM_017024742.1 | 182 | Missense Mutation | AAC,GAC | N,D 13 | XP_016880231.1 | |
XM_017024743.1 | 182 | Missense Mutation | AAC,GAC | N,D 13 | XP_016880232.1 |