Variant #0000948617 (NC_000006.11:g.116441438A>G, NM_000493.3:c.1841T>C (COL10A1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.116441438A>G
DNA change (hg38) -
Published as COL10A1(NM_000493.3):c.1841T>C (p.(Leu614Pro))
ISCN -
DB-ID COL10A1_000028 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL10A1 NM_000493.3 +?/. - c.1841T>C r.(?) p.(Leu614Pro)
NT5DC1 NM_152729.2 +?/. - c.529+2330A>G r.(=) p.(=)


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