Variant #0000720835 (NC_000006.11:g.31918986A>T, NM_006929.4:c.-7984A>T (SKIV2L))

Chromosome 6
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.31918986A>T
DNA change (hg38) -
Published as CFB(NM_001710.5):c.1921A>T (p.T641S)
ISCN -
DB-ID CFB_000028
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFB NM_001710.5 -?/. - c.1921A>T r.(?) p.(Thr641Ser)
NELFE NM_002904.5 -?/. - c.*1092T>A r.(=) p.(=)
SKIV2L NM_006929.4 -?/. - c.-7984A>T r.(?) p.(=)


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