Variant #0000526931 (NC_000006.11:g.116442506C>T, NM_000493.3:c.773G>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.116442506C>T
DNA change (hg38) g.116121343C>T
Published as COL10A1(NM_000493.3):c.773G>A (p.R258Q, p.(Arg258Gln))
ISCN -
DB-ID COL10A1_000011 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) 0.00048 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +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.773G>A r.(?) p.(Arg258Gln)
NT5DC1 NM_152729.2 -?/. - c.529+3398C>T r.(=) p.(=)


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