Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGGAAATGGAGCAGCAGCAGGCCT[A/G]TCGTCCAGGTAGGAAAATACACATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 109135 MIM: 605800 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
AXL 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
|
AXL - AXL receptor tyrosine kinase | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
HNRNPUL1 - heterogeneous nuclear ribonucleoprotein U like 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301016.2 | 740 | Missense Mutation | TAT,TGT | Y,C 48 | NP_001287945.1 | |
NM_001321208.1 | 740 | Missense Mutation | TAT,TGT | Y,C 37 | NP_001308137.1 | |
NM_001321211.1 | 740 | Missense Mutation | TAT,TGT | Y,C 37 | NP_001308140.1 | |
NM_007040.5 | 740 | Missense Mutation | TAT,TGT | Y,C 137 | NP_008971.2 | |
NM_144732.4 | 740 | Missense Mutation | TAT,TGT | Y,C 37 | NP_653333.1 | |
XM_005258459.3 | 740 | Missense Mutation | TAT,TGT | Y,C 137 | XP_005258516.1 | |
XM_005258461.4 | 740 | Missense Mutation | TAT,TGT | Y,C 48 | XP_005258518.1 | |
XM_005258463.3 | 740 | Missense Mutation | TAT,TGT | Y,C 37 | XP_005258520.1 | |
XM_005258464.3 | 740 | Missense Mutation | TAT,TGT | Y,C 37 | XP_005258521.1 | |
XM_005258465.4 | 740 | Missense Mutation | TAT,TGT | Y,C 37 | XP_005258522.1 | |
XM_011526392.2 | 740 | Missense Mutation | TAT,TGT | Y,C 137 | XP_011524694.1 | |
XM_011526393.2 | 740 | Missense Mutation | TAT,TGT | Y,C 37 | XP_011524695.1 | |
XM_011526394.2 | 740 | Missense Mutation | TAT,TGT | Y,C 37 | XP_011524696.1 | |
XM_011526395.2 | 740 | Missense Mutation | TAT,TGT | Y,C 37 | XP_011524697.1 |