Variant #0000268338 (NC_000012.11:g.48398002G>C, COL2A1(NM_001844.4):c.85+18C>G)

Chromosome 12
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.48398002G>C
DNA change (hg38) g.48004219G>C
Published as COL2A1(NM_001844.4):c.85+18C>G, COL2A1(NM_001844.5):c.85+18C>G
ISCN -
DB-ID COL2A1_000402 See all 5 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.74086 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL2A1 NM_001844.4 -/. - c.85+18C>G r.(=) p.(=)