Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGAGCTTGAACTCCATTCCCCGGCC[C/T]GTCCAGGCAATGAAATGGGCATTTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600396 MIM: 600711 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DHX8 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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DHX8 - DEAH-box helicase 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001302623.1 | 532 | Intron | NP_001289552.1 | |||
NM_001322216.1 | 532 | Intron | NP_001309145.1 | |||
NM_001322217.1 | 532 | Intron | NP_001309146.1 | |||
NM_001322218.1 | 532 | Intron | NP_001309147.1 | |||
NM_001322219.1 | 532 | Intron | NP_001309148.1 | |||
NM_001322220.1 | 532 | Intron | NP_001309149.1 | |||
NM_001322221.1 | 532 | Intron | NP_001309150.1 | |||
NM_004941.2 | 532 | Intron | NP_004932.1 |
ETV4 - ETS variant 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001079675.2 | 532 | Silent Mutation | ACA,ACG | T,T 363 | NP_001073143.1 | |
NM_001261437.1 | 532 | Silent Mutation | ACA,ACG | T,T 324 | NP_001248366.1 | |
NM_001261438.1 | 532 | Silent Mutation | ACA,ACG | T,T 324 | NP_001248367.1 | |
NM_001261439.1 | 532 | Silent Mutation | ACA,ACG | T,T 86 | NP_001248368.1 | |
NM_001986.2 | 532 | Silent Mutation | ACA,ACG | T,T 363 | NP_001977.1 | |
XM_011524514.1 | 532 | Silent Mutation | ACA,ACG | T,T 100 | XP_011522816.1 | |
XM_017024349.1 | 532 | Silent Mutation | ACA,ACG | T,T 358 | XP_016879838.1 |