Variant #0000995536 (NC_000006.11:g.1612031_1612032insCCG, NM_001453.2:c.1351_1352insCCG (FOXC1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1612031_1612032insCCG
DNA change (hg38) -
Published as FOXC1(NM_001453.2):c.1351_1352insCCG (p.(Gly450_Gly451insAla)), FOXC1(NM_001453.3):c.1351_1352insCCG (p.G450_G451insA)
ISCN -
DB-ID FOXC1_000040 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FOXC1 NM_001453.2 -?/. - c.1351_1352insCCG r.(?) p.(Gly450_Gly451insAla)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.