Variant #0000912389 (NC_000006.11:g.116441718T>A, NM_000493.3:c.1561A>T (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.116441718T>A
DNA change (hg38) -
Published as COL10A1(NM_000493.3):c.1561A>T (p.(Met521Leu))
ISCN -
DB-ID COL10A1_000025
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) 2.0E-5 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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL10A1 NM_000493.3 -?/. - c.1561A>T r.(?) p.(Met521Leu)
NT5DC1 NM_152729.2 -?/. - c.529+2610T>A r.(=) p.(=)


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