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TCAGCGCACGACAGTCACGTGGGGA[A/G]GGGCAGTGGCCAGGTCGGCCTTGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
6 submissions
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Phenotype: |
MIM: 615242 | ||||||||||||||||||||
Literature Links: |
CCDC27 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
CCDC27 - coiled-coil domain containing 27 | ||||||
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There are no transcripts associated with this gene. |
LRRC47 - leucine rich repeat containing 47 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020710.2 | 1755 | Missense Mutation | CCT,CTT | P,L 576 | NP_065761.1 |
SMIM1 - small integral membrane protein 1 (Vel blood group) | ||||||
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There are no transcripts associated with this gene. |