Variant #0000990666 (NC_000001.10:g.196642977_196642978dup, NC_000001.10(NM_000186.3):c.245-10_245-9dup (CFH))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.196642977_196642978dup
DNA change (hg38) -
Published as CFH(NM_000186.3):c.245-10_245-9dupTT (p.?), CFH(NM_000186.3):c.245-11_245-10dupTT, CFH(NM_000186.4):c.245-10_245-9dupTT
ISCN -
DB-ID CFH_000052 See all 3 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFH NM_000186.3 -/. - c.245-10_245-9dup r.(=) p.(=)


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