Variant #0000273780 (NC_000001.10:g.103496816_103496818dup, NC_000001.10(NM_001854.3):c.652-8_652-6dup (COL11A1))

Chromosome 1
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.103496816_103496818dup
DNA change (hg38) g.103031260_103031262dup
Published as COL11A1(NM_001190709.1):c.652-6_652-5insTTT (p.(=)), COL11A1(NM_001854.4):c.652-9_652-7dupTTT, COL11A1(NM_080629.2):c.652-8_652-6dupTTT, COL11A1(N...)
ISCN -
DB-ID COL11A1_000086 See all 5 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL11A1 NM_001854.3 -?/. - c.652-8_652-6dup r.(=) p.(=)


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