Product Details

SNP ID

hCV11926459

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:113110806 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGGGAGTGCAAGGAGGAGCAGTGC[C/T]CCTTCGAGGAGGCCCGGGAGATCTT

Phenotype

MIM: 613878

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

F7 PubMed Links

Gene Details

Gene

F7

Gene Name

coagulation factor VII

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000131.4	235	Missense Mutation	CCC,TCC	P83S	NP_000122.1
NM_001267554.1	235	Intron			NP_001254483.1
NM_019616.3	235	Missense Mutation	CCC,TCC	P61S	NP_062562.1

View Full Product Details