Variant #0000322769 (NC_000012.11:g.48367327C>T, NM_001844.4:c.4327G>A (COL2A1))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.48367327C>T
DNA change (hg38) g.47973544C>T
Published as COL2A1(NM_001844.4):c.4327G>A (p.(Gly1443Ser)), COL2A1(NM_001844.5):c.4327G>A (p.G1443S)
ISCN -
DB-ID COL2A1_000393 See all 3 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) 0.00096 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 2018-01-15 20:58:59 +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     
COL2A1 NM_001844.4 ?/. - c.4327G>A r.(?) p.(Gly1443Ser)
TMEM106C NM_024056.3 ?/. - c.*5315C>T r.(=) p.(=)


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