Variant #0000853116 (NC_000011.9:g.66605858G>A, NM_024650.3:c.1689G>A (C11orf80))

Chromosome 11
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.66605858G>A
DNA change (hg38) -
Published as C11orf80(NM_024650.3):c.1689G>A (p.K563=)
ISCN -
DB-ID C11orf80_000028
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) 1.0E-5 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 15:40:45 +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     
RCE1 NM_005133.2 -?/. - c.-5069G>A r.(?) p.(=)
C11orf80 NM_024650.3 -?/. - c.1689G>A r.(?) p.(Lys563=)


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