Variant #0000655472 (NC_000006.11:g.116446576A>G, NM_000493.3:c.80T>C (COL10A1))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.116446576A>G
DNA change (hg38) g.116125413A>G
Published as COL10A1(NM_000493.4):c.80T>C (p.M27T), NT5DC1(NM_152729.3):c.529+7468A>G
ISCN -
DB-ID COL10A1_000003 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) 0.36931 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.80T>C r.(?) p.(Met27Thr)
NT5DC1 NM_152729.2 -/. - c.529+7468A>G r.(=) p.(=)


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