Variant #0000805326 (NC_000011.9:g.66617523C>T, NM_001040716.1:c.2783G>A (PC))

Chromosome 11
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.66617523C>T
DNA change (hg38) -
Published as PC(NM_001040716.1):c.2783G>A (p.R928Q)
ISCN -
DB-ID C11orf80_000025
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) 0.00012 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 2021-09-17 14:40:49 +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     
PC NM_001040716.1 ?/. - c.2783G>A r.(?) p.(Arg928Gln)
RCE1 NM_005133.2 ?/. - c.*3957C>T r.(=) p.(=)
LRFN4 NM_024036.4 ?/. - c.-7693C>T r.(?) p.(=)
C11orf80 NM_024650.3 ?/. - c.*6818C>T r.(=) p.(=)


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