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TTCACCATACCGCACGGGTCCTGCT[C/G]GCTGACCCAGCCCGCCTGCTGTCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607139 MIM: 609217 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FANCA 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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FANCA - Fanconi anemia complementation group A | ||||||
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There are no transcripts associated with this gene. |
LOC107984817 - uncharacterized LOC107984817 | ||||||
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There are no transcripts associated with this gene. |
SPIRE2 - spire type actin nucleation factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032451.1 | Intron | NP_115827.1 | ||||
XM_011523379.1 | Intron | XP_011521681.1 | ||||
XM_011523380.2 | Intron | XP_011521682.1 | ||||
XM_011523381.1 | Intron | XP_011521683.1 | ||||
XM_011523384.1 | Intron | XP_011521686.1 | ||||
XM_011523385.1 | Intron | XP_011521687.1 | ||||
XM_017023779.1 | Intron | XP_016879268.1 | ||||
XM_017023780.1 | Intron | XP_016879269.1 | ||||
XM_017023781.1 | Intron | XP_016879270.1 |