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CGCCCAGCTGCGTGGCGAGGCAGCG[A/G]CCCAGCAGCGCTTTGCCCGCGCCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600702 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FIGNL2 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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FIGNL2 - fidgetin like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001013690.4 | 1740 | Silent Mutation | GGC,GGT | G,G 442 | NP_001013712.4 | |
XM_005268870.3 | 1740 | Silent Mutation | GGC,GGT | G,G 442 | XP_005268927.1 | |
XM_017019298.1 | 1740 | Silent Mutation | GGC,GGT | G,G 556 | XP_016874787.1 | |
XM_017019299.1 | 1740 | Silent Mutation | GGC,GGT | G,G 540 | XP_016874788.1 |
SCN8A - sodium voltage-gated channel alpha subunit 8 | ||||||
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There are no transcripts associated with this gene. |