Variant #0000504574 (NC_000001.10:g.196795998_196796002del, NM_002113.2:c.293_297del (CFHR1))

Chromosome 1
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.196795998_196796002del
DNA change (hg38) g.196826868_196826872del
Published as CFHR1(NM_002113.2):c.293_297del (p.(Glu98ValfsTer9))
ISCN -
DB-ID CFHR1_000012
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFHR1 NM_002113.2 ?/. - c.293_297del r.(?) p.(Glu98ValfsTer9)


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