Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGGCTTTCTCGATATCGGGGTGCA[C/T]GGCCTGTGGAAGCCACTCACAGTAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
DHX37 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
|
DHX37 - DEAH-box helicase 37 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032656.3 | 3526 | Missense Mutation | ATG,GTG | M,V 1143 | NP_116045.2 | |
XM_005253590.3 | 3526 | Intron | XP_005253647.1 | |||
XM_011538598.2 | 3526 | Intron | XP_011536900.1 | |||
XM_011538600.2 | 3526 | Intron | XP_011536902.1 |