Variant #0000504614 (NC_000001.10:g.196963265dup, NM_030787.3:c.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.196963265dup
DNA change (hg38) g.196994135dup
Published as CFHR5(NM_030787.3):c.486dup (p.(Glu163ArgfsTer35)), CFHR5(NM_030787.3):c.486dupA (p.E163Rfs*35), CFHR5(NM_030787.4):c.486dupA (p.E163Rfs*35)
ISCN -
DB-ID CFHR5_000003 See all 5 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_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 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.486dup r.(?) p.(Glu163ArgfsTer35)


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