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GCAGAAAGTGTTGACACTGGAAGAA[C/T]GTTGCAGCAAATTAGAAGGTCAGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613481 MIM: 604550 | ||||||||||||||||||||
Literature Links: |
CCDC62 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 |
CCDC62 - coiled-coil domain containing 62 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_201435.4 | 1261 | Missense Mutation | CGT,TGT | R,C 71 | NP_958843.2 | |
XM_006719643.1 | 1261 | Missense Mutation | CGT,TGT | R,C 71 | XP_006719706.1 | |
XM_006719644.1 | 1261 | Missense Mutation | CGT,TGT | R,C 71 | XP_006719707.1 | |
XM_011538856.1 | 1261 | Missense Mutation | CGT,TGT | R,C 71 | XP_011537158.1 | |
XM_011538857.1 | 1261 | Missense Mutation | CGT,TGT | R,C 71 | XP_011537159.1 | |
XM_011538859.1 | 1261 | Intron | XP_011537161.1 | |||
XM_017020033.1 | 1261 | Missense Mutation | CGT,TGT | R,C 71 | XP_016875522.1 |
DENR - density regulated re-initiation and release factor | ||||||
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There are no transcripts associated with this gene. |