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AAAAAAAACAAAACAACAACAACAA[A/C]AAAAAAACACTGTATGTTAAGGGAG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 616493 | |||||||||||||||||||||||
Literature Links: |
CCDC66 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 |
FAM208A - family with sequence similarity 208 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001112736.1 | 6193 | UTR 3 | NP_001106207.1 | |||
NM_015224.3 | 6193 | UTR 3 | NP_056039.2 | |||
XM_005264999.1 | 6193 | UTR 3 | XP_005265056.1 | |||
XM_006713077.2 | 6193 | Intron | XP_006713140.1 | |||
XM_006713078.2 | 6193 | Intron | XP_006713141.1 | |||
XM_011533552.2 | 6193 | Intron | XP_011531854.1 | |||
XM_011533553.2 | 6193 | Intron | XP_011531855.1 | |||
XM_017006030.1 | 6193 | Intron | XP_016861519.1 | |||
XM_017006031.1 | 6193 | Intron | XP_016861520.1 | |||
XM_017006032.1 | 6193 | Intron | XP_016861521.1 |