Variant #0000862655 (NC_000011.9:g.66610422C>T, NM_024650.3:c.1850C>T (C11orf80))

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.66610422C>T
DNA change (hg38) -
Published as C11orf80(NM_024650.3):c.1850C>T (p.A617V)
ISCN -
DB-ID C11orf80_000029
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_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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RCE1 NM_005133.2 ?/. - c.-505C>T r.(?) p.(=)
C11orf80 NM_024650.3 ?/. - c.1850C>T r.(?) p.(Ala617Val)


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