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GCTGCAGCCGCACGCGGAGCCCGGC[G/T]GCTACTCGGGGCCGGACGGACATTG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 109135 MIM: 605800 | |||||||||||||||||||||||
Literature Links: |
AXL PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba)
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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 |
AXL - AXL receptor tyrosine kinase | ||||||
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There are no transcripts associated with this gene. |
HNRNPUL1 - heterogeneous nuclear ribonucleoprotein U like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301016.2 | 601 | Intron | NP_001287945.1 | |||
NM_001321208.1 | 601 | Intron | NP_001308137.1 | |||
NM_001321211.1 | 601 | Intron | NP_001308140.1 | |||
NM_007040.5 | 601 | Missense Mutation | GGC,TGC | G,C 91 | NP_008971.2 | |
NM_144732.4 | 601 | Intron | NP_653333.1 | |||
XM_005258459.3 | 601 | Missense Mutation | GGC,TGC | G,C 91 | XP_005258516.1 | |
XM_005258461.4 | 601 | Intron | XP_005258518.1 | |||
XM_005258463.3 | 601 | Intron | XP_005258520.1 | |||
XM_005258464.3 | 601 | Intron | XP_005258521.1 | |||
XM_005258465.4 | 601 | Intron | XP_005258522.1 | |||
XM_011526392.2 | 601 | Missense Mutation | GGC,TGC | G,C 91 | XP_011524694.1 | |
XM_011526393.2 | 601 | Intron | XP_011524695.1 | |||
XM_011526394.2 | 601 | Intron | XP_011524696.1 | |||
XM_011526395.2 | 601 | Intron | XP_011524697.1 |