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CAGAGGCGCTAAAGAGGAGCACGGT[A/G]GACTGATGTGAGCTTCTCTTCCTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613478 MIM: 191318 | ||||||||||||||||||||
Literature Links: |
CCDC106 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 |
CCDC106 - coiled-coil domain containing 106 | ||||||
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There are no transcripts associated with this gene. |
U2AF2 - U2 small nuclear RNA auxiliary factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012478.1 | 1316 | Missense Mutation | AGA,GGA | R,G 75 | NP_001012496.1 | |
NM_007279.2 | 1316 | Missense Mutation | AGA,GGA | R,G 75 | NP_009210.1 | |
XM_006722994.2 | 1316 | UTR 5 | XP_006723057.1 | |||
XM_011526410.1 | 1316 | UTR 5 | XP_011524712.1 |