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CCCCTCCCCCGCGCCTGTGTCCCCA[A/G]GGCGCAGGGCCGCGCGTCCAGCCCC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 607891 | |||||||||||||||||||||||
Literature Links: |
CMTM8 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
CMTM8 - CKLF like MARVEL transmembrane domain containing 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320308.1 | 220 | UTR 5 | NP_001307237.1 | |||
NM_178868.4 | 220 | UTR 5 | NP_849199.2 | |||
XM_011533416.2 | 220 | Intron | XP_011531718.1 | |||
XM_017005779.1 | 220 | Intron | XP_016861268.1 | |||
XM_017005780.1 | 220 | Intron | XP_016861269.1 |