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AGCTCACACACACTGAAGCTGGCAC[A/G]GATGGAGTCTTTGACAGTGTTTTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 608170 MIM: 615813 | ||||||||||||||||||||
Literature Links: |
DDX41 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
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 |
DDX41 - DEAD-box helicase 41 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
FAM193B - family with sequence similarity 193 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001190946.2 | 2291 | Missense Mutation | CGT,TGT | R,C 487 | NP_001177875.1 | |
XM_006714875.2 | 2291 | Missense Mutation | CGT,TGT | R,C 567 | XP_006714938.1 | |
XM_006714876.1 | 2291 | Missense Mutation | CGT,TGT | R,C 454 | XP_006714939.1 | |
XM_006714878.1 | 2291 | Missense Mutation | CGT,TGT | R,C 454 | XP_006714941.1 | |
XM_006714879.3 | 2291 | Missense Mutation | CGT,TGT | R,C 454 | XP_006714942.1 | |
XM_006714880.1 | 2291 | Missense Mutation | CGT,TGT | R,C 454 | XP_006714943.1 | |
XM_006714884.1 | 2291 | Missense Mutation | CGT,TGT | R,C 113 | XP_006714947.1 | |
XM_006714885.1 | 2291 | Missense Mutation | CGT,TGT | R,C 113 | XP_006714948.1 | |
XM_006714886.2 | 2291 | Intron | XP_006714949.1 | |||
XM_011534572.1 | 2291 | Missense Mutation | CGT,TGT | R,C 532 | XP_011532874.1 | |
XM_011534573.1 | 2291 | Missense Mutation | CGT,TGT | R,C 523 | XP_011532875.1 | |
XM_011534574.1 | 2291 | Missense Mutation | CGT,TGT | R,C 489 | XP_011532876.1 | |
XM_011534579.2 | 2291 | Missense Mutation | CGT,TGT | R,C 462 | XP_011532881.1 | |
XM_011534580.1 | 2291 | Missense Mutation | CGT,TGT | R,C 454 | XP_011532882.1 | |
XM_011534581.1 | 2291 | Missense Mutation | CGT,TGT | R,C 251 | XP_011532883.1 | |
XM_011534582.1 | 2291 | Missense Mutation | CGT,TGT | R,C 113 | XP_011532884.1 | |
XM_011534583.1 | 2291 | Missense Mutation | CGT,TGT | R,C 113 | XP_011532885.1 |