Variant #0000266884 (NC_000006.11:g.116441230_116441231insGGG, NM_000493.3:c.*6_*7insCCC (COL10A1))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.116441230_116441231insGGG
DNA change (hg38) g.116120067_116120068insGGG
Published as COL10A1(NM_000493.4):c.*5_*6insCCC, NT5DC1(NM_152729.3):c.529+2122_529+2123insGGG
ISCN -
DB-ID COL10A1_000001
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL10A1 NM_000493.3 -/. - c.*6_*7insCCC r.(=) p.(=)
NT5DC1 NM_152729.2 -/. - c.529+2122_529+2123insGGG r.(=) p.(=)


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