Product Details

SNP ID
rs199769643
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:17864636 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAATCATTTGGCCTAATTTTCATAA[C/T]CACAGATTTCAGAGAATACCACCAC
Phenotype
MIM: 605776
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FGL1 PubMed Links

Gene Details

Gene
FGL1
Gene Name
fibrinogen like 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004467.3 1004 Missense Mutation NP_004458.3
NM_147203.2 1004 Missense Mutation NP_671736.2
NM_201552.1 1004 Missense Mutation NP_963846.1
NM_201553.1 1004 Missense Mutation NP_963847.1
XM_017013232.1 1004 Missense Mutation XP_016868721.1
XM_017013233.1 1004 Missense Mutation XP_016868722.1

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