Variant #0000689610 (NC_000006.11:g.116446506A>T, NM_000493.3:c.150T>A (COL10A1))

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.116446506A>T
DNA change (hg38) -
Published as COL10A1(NM_000493.3):c.150T>A (p.S50R, p.(Ser50Arg))
ISCN -
DB-ID COL10A1_000015 See all 3 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) 0.00383 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL10A1 NM_000493.3 -?/. - c.150T>A r.(?) p.(Ser50Arg)
NT5DC1 NM_152729.2 -?/. - c.529+7398A>T r.(=) p.(=)


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