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GTTATAATATGGGAGTGCTTGCCCT[C/T]GCCATATCCGAGGAACCTGGGACTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615383 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FIGNL1 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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FIGNL1 - fidgetin like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042762.2 | 6774 | Intron | NP_001036227.1 | |||
NM_001287492.1 | 6774 | Intron | NP_001274421.1 | |||
NM_001287493.1 | 6774 | Intron | NP_001274422.1 | |||
NM_001287494.1 | 6774 | Intron | NP_001274423.1 | |||
NM_001287495.1 | 6774 | Intron | NP_001274424.1 | |||
NM_001287496.1 | 6774 | Intron | NP_001274425.1 | |||
NM_022116.4 | 6774 | Intron | NP_071399.2 | |||
XM_011515470.2 | 6774 | UTR 3 | XP_011513772.1 | |||
XM_017012501.1 | 6774 | UTR 3 | XP_016867990.1 | |||
XM_017012502.1 | 6774 | UTR 3 | XP_016867991.1 |