Variant #0000545282 (NC_000011.9:g.66512305_66512316dup, NM_024650.3:c.92_103dup (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.66512305_66512316dup
DNA change (hg38) g.66744834_66744845dup
Published as C11orf80(NM_024650.3):c.92_103dupCGGCGGCGGCGG (p.A31_A34dup)
ISCN -
DB-ID C11orf80_000010
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RCE1 NM_005133.2 ?/. - c.-98622_-98611dup r.(?) p.(=)
C11orf80 NM_024650.3 ?/. - c.92_103dup r.(?) p.(Ala31_Ala34dup)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.