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ATATGGGTCTTACCCTGCCTGTCCC[A/G]GGGAGTTCCAGTAAGGATTGTCTAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616047 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CFAP97 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CFAP97 - cilia and flagella associated protein 97 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001292033.1 | Intron | NP_001278962.1 | ||||
NM_020827.2 | Intron | NP_065878.1 | ||||
XM_017008483.1 | Intron | XP_016863972.1 | ||||
XM_017008484.1 | Intron | XP_016863973.1 | ||||
XM_017008485.1 | Intron | XP_016863974.1 | ||||
XM_017008486.1 | Intron | XP_016863975.1 |
SNX25 - sorting nexin 25 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317781.1 | Intron | NP_001304710.1 | ||||
XM_005263267.4 | Intron | XP_005263324.1 | ||||
XM_011532302.2 | Intron | XP_011530604.1 | ||||
XM_011532303.2 | Intron | XP_011530605.1 | ||||
XM_011532304.2 | Intron | XP_011530606.1 | ||||
XM_011532305.2 | Intron | XP_011530607.1 | ||||
XM_011532306.2 | Intron | XP_011530608.1 | ||||
XM_011532307.2 | Intron | XP_011530609.1 | ||||
XM_011532308.2 | Intron | XP_011530610.1 | ||||
XM_017008680.1 | Intron | XP_016864169.1 | ||||
XM_017008681.1 | Intron | XP_016864170.1 | ||||
XM_017008682.1 | Intron | XP_016864171.1 | ||||
XM_017008683.1 | Intron | XP_016864172.1 | ||||
XM_017008684.1 | Intron | XP_016864173.1 | ||||
XM_017008685.1 | Intron | XP_016864174.1 | ||||
XM_017008686.1 | Intron | XP_016864175.1 | ||||
XM_017008687.1 | Intron | XP_016864176.1 |