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CCCTCGACTGCAGTCCTCCAGGGCC[C/T]GGCCGAGGTGGGGAGCCAAATCGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611204 MIM: 601404 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC88C 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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CCDC88C - coiled-coil domain containing 88C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080414.3 | 3198 | Missense Mutation | NP_001073883.2 | |||
XM_005267691.4 | 3198 | Intron | XP_005267748.1 | |||
XM_011536796.2 | 3198 | Missense Mutation | XP_011535098.1 | |||
XM_017021335.1 | 3198 | Intron | XP_016876824.1 | |||
XM_017021336.1 | 3198 | Missense Mutation | XP_016876825.1 | |||
XM_017021337.1 | 3198 | Intron | XP_016876826.1 |
GPR68 - G protein-coupled receptor 68 | ||||||
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There are no transcripts associated with this gene. |