Variant #0000883013 (NC_000001.10:g.196963264_196963265dup, NM_030787.3:c.485_486dup (CFHR5))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.196963264_196963265dup
DNA change (hg38) -
Published as CFHR5(NM_030787.3):c.485_486dupAA (p.E163Kfs*10), CFHR5(NM_030787.4):c.485_486dupAA (p.E163Kfs*10)
ISCN -
DB-ID CFHR5_000019 See all 4 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFHR5 NM_030787.3 -?/. - c.485_486dup r.(?) p.(Glu163LysfsTer10)


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