Variant #0000526929 (NC_000006.11:g.116442414T>C, NM_000493.3:c.865A>G (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.116442414T>C
DNA change (hg38) g.116121251T>C
Published as COL10A1(NM_000493.3):c.865A>G (p.(Ile289Val))
ISCN -
DB-ID COL10A1_000009
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) 0.00016 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL10A1 NM_000493.3 -?/. - c.865A>G r.(?) p.(Ile289Val)
NT5DC1 NM_152729.2 -?/. - c.529+3306T>C r.(=) p.(=)


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