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GGTACTGGGCCTCCAGGGTACTGTC[A/G]TTGGCCGGGCCGGGCCAGCTCAAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608170 MIM: 611435 MIM: 605903 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DDX41 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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DDX41 - DEAD-box helicase 41 | ||||||
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There are no transcripts associated with this gene. |
DOK3 - docking protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144875.1 | 1251 | Intron | NP_001138347.1 | |||
NM_001144876.1 | 1251 | Intron | NP_001138348.1 | |||
NM_001308235.1 | 1251 | Silent Mutation | AAC,AAT | N,N 389 | NP_001295164.1 | |
NM_001308236.1 | 1251 | Silent Mutation | AAC,AAT | N,N 389 | NP_001295165.1 | |
NM_024872.2 | 1251 | Silent Mutation | AAC,AAT | N,N 445 | NP_079148.2 | |
XM_005265985.3 | 1251 | Silent Mutation | AAC,AAT | N,N 389 | XP_005266042.1 | |
XM_005265987.1 | 1251 | Intron | XP_005266044.1 | |||
XM_011534654.2 | 1251 | Silent Mutation | AAC,AAT | N,N 389 | XP_011532956.1 | |
XM_011534655.2 | 1251 | Silent Mutation | AAC,AAT | N,N 389 | XP_011532957.1 | |
XM_011534656.2 | 1251 | Silent Mutation | AAC,AAT | N,N 389 | XP_011532958.1 | |
XM_011534657.2 | 1251 | Silent Mutation | AAC,AAT | N,N 287 | XP_011532959.1 | |
XM_017009883.1 | 1251 | Silent Mutation | AAC,AAT | N,N 344 | XP_016865372.1 | |
XM_017009884.1 | 1251 | Intron | XP_016865373.1 |
PDLIM7 - PDZ and LIM domain 7 | ||||||
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There are no transcripts associated with this gene. |