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TCGCGGCCGGTGCTGGAGGGGCTGC[A/G]GGCGGCCGGCTTCGAGAGGCCCTCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
6 submissions
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Phenotype: |
MIM: 606168 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DDX20 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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DDX20 - DEAD-box helicase 20 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_007204.4 | 590 | Missense Mutation | CAG,CGG | Q,R 78 | NP_009135.4 |
FAM212B - family with sequence similarity 212 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_019099.4 | 590 | Intron | NP_061972.1 | |||
NM_198926.2 | 590 | Intron | NP_945120.1 | |||
XM_011541783.2 | 590 | Intron | XP_011540085.1 |
FAM212B-AS1 - FAM212B antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |
LOC101928718 - uncharacterized LOC101928718 | ||||||
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There are no transcripts associated with this gene. |