Variant #0000089878 (NC_000006.11:g.6266862G>A, NM_000129.3:c.500C>T (F13A1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.6266862G>A
DNA change (hg38) g.6266629G>A
Published as Pro166Leu
ISCN -
DB-ID F13A1_000012
Variant remarks expression cloning COS-1 cells
Reference PubMed: Thomas 2016, Journal: Thomas 2016
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation ?
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Arijit Biswas
Database submission license No license selected
Created by Arijit Biswas
Date created 2016-02-24 13:37:24 +01:00 (CET)
Date last edited 2019-07-09 13:56:51 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
F13A1 NM_000129.3 +?/. - c.500C>T r.(?) p.(Pro167Leu)


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