Variant #0000724039 (NC_000012.11:g.48367218A>G, NM_001844.4:c.4436T>C (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.48367218A>G
DNA change (hg38) -
Published as COL2A1(NM_001844.4):c.4436T>C (p.(Val1479Ala))
ISCN -
DB-ID COL2A1_000690 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 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 2021-02-08 18:36:18 +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     
COL2A1 NM_001844.4 ?/. - c.4436T>C r.(?) p.(Val1479Ala)
TMEM106C NM_024056.3 ?/. - c.*5206A>G r.(=) p.(=)


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