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TGGATTGGAAAGATGATTTACTCTC[A/G]GGAATCTTCTCTGTCAGCCTGTACA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601731 MIM: 135600 | ||||||||||||||||||||
Literature Links: |
ATIC PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ATIC - 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase | ||||||
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There are no transcripts associated with this gene. |
FN1 - fibronectin 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001306129.1 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2445 | NP_001293058.1 | |
NM_001306130.1 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2266 | NP_001293059.1 | |
NM_001306131.1 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2264 | NP_001293060.1 | |
NM_001306132.1 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2239 | NP_001293061.1 | |
NM_002026.3 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2354 | NP_002017.1 | |
NM_054034.2 | 7149 | Intron | NP_473375.2 | |||
NM_212474.2 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2175 | NP_997639.1 | |
NM_212476.2 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2295 | NP_997641.1 | |
NM_212478.2 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2329 | NP_997643.1 | |
NM_212482.2 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2476 | NP_997647.1 | |
XM_005246397.1 | 7149 | Intron | XP_005246454.1 | |||
XM_005246398.1 | 7149 | Intron | XP_005246455.1 | |||
XM_005246399.1 | 7149 | Intron | XP_005246456.1 | |||
XM_005246401.1 | 7149 | Intron | XP_005246458.1 | |||
XM_005246402.1 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2420 | XP_005246459.1 | |
XM_005246403.1 | 7149 | Intron | XP_005246460.1 | |||
XM_005246404.1 | 7149 | Intron | XP_005246461.1 | |||
XM_005246405.1 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2386 | XP_005246462.1 | |
XM_005246406.1 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2385 | XP_005246463.1 | |
XM_005246407.1 | 7149 | Intron | XP_005246464.1 | |||
XM_005246408.1 | 7149 | Intron | XP_005246465.1 | |||
XM_005246409.1 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2360 | XP_005246466.1 | |
XM_005246410.1 | 7149 | Intron | XP_005246467.1 | |||
XM_005246411.1 | 7149 | Intron | XP_005246468.1 | |||
XM_005246412.1 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2270 | XP_005246469.1 | |
XM_005246414.1 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2265 | XP_005246471.1 | |
XM_005246416.1 | 7149 | Intron | XP_005246473.1 | |||
XM_017003692.1 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2356 | XP_016859181.1 | |
XM_017003693.1 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2355 | XP_016859182.1 | |
XM_017003694.1 | 7149 | Nonsense Mutation | CGA,TGA | R,* 2330 | XP_016859183.1 | |
XM_017003695.1 | 7149 | Intron | XP_016859184.1 |