Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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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. |
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 | 1033 | Intron | NP_115827.1 | |||
XM_011523379.1 | 1033 | Missense Mutation | GAA,GGA | E,G 19 | XP_011521681.1 | |
XM_011523380.2 | 1033 | Intron | XP_011521682.1 | |||
XM_011523381.1 | 1033 | UTR 5 | XP_011521683.1 | |||
XM_011523384.1 | 1033 | Intron | XP_011521686.1 | |||
XM_011523385.1 | 1033 | Intron | XP_011521687.1 | |||
XM_017023779.1 | 1033 | Intron | XP_016879268.1 | |||
XM_017023780.1 | 1033 | Intron | XP_016879269.1 | |||
XM_017023781.1 | 1033 | Intron | XP_016879270.1 |
Set Membership: |
HapMap |