Variant #0000337807 (NC_000006.11:g.33160217C>T, NM_080680.2:c.-200G>A (COL11A2))

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.33160217C>T
DNA change (hg38) g.33192440C>T
Published as -
ISCN -
DB-ID COL11A2_000074
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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A7 NM_006979.2 -/. - c.-8806C>T r.(?) p.(=)
RXRB NM_021976.4 -/. - c.*2242G>A r.(=) p.(=)
COL11A2 NM_080680.2 -/. - c.-200G>A r.(?) p.(=)


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