Product Details

SNP ID

hCV11926455

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:113110749 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCACCGGCGCCGGCGCGCCAACGCG[C/T]TCCTGGAGGAGCTGCGGCCGGGCTC

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	178	Missense Mutation	CTC,TTC	L64F	NP_000122.1
NM_001267554.1	178	Intron			NP_001254483.1
NM_019616.3	178	Missense Mutation	CTC,TTC	L42F	NP_062562.1

View Full Product Details