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TGCTTGTTGAGTAACACATTTTTAT[C/T]TGGAGATAGTGTCTTACTAAGTCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607570 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DHX40 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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DHX40 - DEAH-box helicase 40 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001166301.1 | Intron | NP_001159773.1 | ||||
NM_024612.4 | Intron | NP_078888.4 | ||||
XM_006722083.2 | Intron | XP_006722146.1 | ||||
XM_011525253.2 | Intron | XP_011523555.1 | ||||
XM_011525254.2 | Intron | XP_011523556.1 | ||||
XM_017025080.1 | Intron | XP_016880569.1 | ||||
XM_017025081.1 | Intron | XP_016880570.1 | ||||
XM_017025082.1 | Intron | XP_016880571.1 | ||||
XM_017025083.1 | Intron | XP_016880572.1 |