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TTACATTTGGAATAAAATCATTTGG[A/C]CTAATTTTCATAACCACAGATTTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605776 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FGL1 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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FGL1 - fibrinogen like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004467.3 | 1018 | Missense Mutation | AGG,AGT | R,S 303 | NP_004458.3 | |
NM_147203.2 | 1018 | Missense Mutation | AGG,AGT | R,S 303 | NP_671736.2 | |
NM_201552.1 | 1018 | Missense Mutation | AGG,AGT | R,S 303 | NP_963846.1 | |
NM_201553.1 | 1018 | Missense Mutation | AGG,AGT | R,S 303 | NP_963847.1 | |
XM_017013232.1 | 1018 | Missense Mutation | AGG,AGT | R,S 303 | XP_016868721.1 | |
XM_017013233.1 | 1018 | Missense Mutation | AGG,AGT | R,S 273 | XP_016868722.1 |