Variant #0000273797 (NC_000006.11:g.33156845C>G, NM_080680.2:c.353G>C (COL11A2))

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.33156845C>G
DNA change (hg38) g.33189068C>G
Published as COL11A2(NM_001163771.1):c.353G>C (p.(Arg118Pro)), COL11A2(NM_080680.2):c.353G>C (p.R118P)
ISCN -
DB-ID COL11A2_000058 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) 0.0021 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A7 NM_006979.2 -?/. - c.-12178C>G r.(?) p.(=)
RXRB NM_021976.4 -?/. - c.*5614G>C r.(=) p.(=)
COL11A2 NM_080680.2 -?/. - c.353G>C r.(?) p.(Arg118Pro)


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