Variant #0000860318 (NC_000006.11:g.33157099G>T, NM_080680.2:c.230C>A (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.33157099G>T
DNA change (hg38) -
Published as COL11A2(NM_001163771.1):c.230C>A (p.(Pro77Gln)), COL11A2(NM_080680.2):c.230C>A (p.P77Q)
ISCN -
DB-ID RXRB_000005 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) 0.00092 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 2022-05-09 15:51:19 +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.-11924G>T r.(?) p.(=)
RXRB NM_021976.4 ?/. - c.*5360C>A r.(=) p.(=)
COL11A2 NM_080680.2 ?/. - c.230C>A r.(?) p.(Pro77Gln)


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