Variant #0001035728 (NC_000006.11:g.33156764G>C, NM_080680.2:c.434C>G (COL11A2))

Chromosome 6
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.33156764G>C
DNA change (hg38) -
Published as COL11A2(NM_080680.2):c.434C>G (p.A145G), COL11A2(NM_080680.3):c.434C>G (p.A145G)
ISCN -
DB-ID RXRB_000003 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) 4.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A7 NM_006979.2 ?/. - c.-12259G>C r.(?) p.(=)
RXRB NM_021976.4 ?/. - c.*5695C>G r.(=) p.(=)
COL11A2 NM_080680.2 ?/. - c.434C>G r.(?) p.(Ala145Gly)


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