Product Details

SNP ID

rs189409610

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:113106846 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCCCGGCCACCTTCCTGCCCCAGG[C/T]GGGGTCGCTAAGGCCTCAGGAGGAG

Phenotype

MIM: 613878 MIM: 609499

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	120	Silent Mutation	GGC,GGT	G22G	NP_000122.1
NM_001267554.1	120	Intron			NP_001254483.1
NM_019616.3	120	Intron			NP_062562.1
XM_006719963.3	120	Intron			XP_006720026.2
XM_011537474.2	120	Intron			XP_011535776.2
XM_011537475.2	120	Intron			XP_011535777.2
XM_011537476.2	120	Intron			XP_011535778.1

Gene

MCF2L

Gene Name

MCF.2 cell line derived transforming sequence like

There are no transcripts associated with this gene.

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