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SNP ID: rs200265489
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:15385030 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TAGTTCCCAATCTTTGATTTCCAGG[A/T]TTTGGCCCTTTCAAACCCATTTTTT
Phenotype: MIM: 300091 MIM: 300931
Polymorphism: A/T, Transversion substitution
Allele Nomenclature
Literature Links: FIGF PubMed Links

Gene Details

Gene: FIGF
Gene Name: c-fos induced growth factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004469.4	1332	Intron			NP_004460.1

Gene: PIR
Gene Name: pirin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001018109.2	1332	Missense Mutation	ACC,TCC	T283S	NP_001018119.1
NM_003662.3	1332	Missense Mutation	ACC,TCC	T283S	NP_003653.1

Gene: PIR-FIGF
Gene Name: PIR-FIGF readthrough

There are no transcripts associated with this gene.

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