Variant #0000545281 (NC_000011.9:g.66512297_66512298insCCG, NM_024650.3:c.84_85insCCG (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.66512297_66512298insCCG
DNA change (hg38) g.66744826_66744827insCCG
Published as C11orf80(NM_024650.3):c.84_85insCCG (p.A28_A29insP)
ISCN -
DB-ID C11orf80_000009
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RCE1 NM_005133.2 ?/. - c.-98630_-98629insCCG r.(?) p.(=)
C11orf80 NM_024650.3 ?/. - c.84_85insCCG r.(?) p.(Ala28_Ala29insPro)


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