Variant #0000912451 (NC_000006.11:g.31914890C>T, NM_006929.4:c.-12080C>T (SKIV2L))

Chromosome 6
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.31914890C>T
DNA change (hg38) -
Published as CFB(NM_001710.5):c.405C>T (p.Y135=)
ISCN -
DB-ID CFB_000016 See all 2 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) 0.00353 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +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     
C2 NM_000063.4 -/. - c.*1756C>T r.(=) p.(=)
CFB NM_001710.5 -/. - c.405C>T r.(?) p.(Tyr135=)
NELFE NM_002904.5 -/. - c.*5188G>A r.(=) p.(=)
SKIV2L NM_006929.4 -/. - c.-12080C>T r.(?) p.(=)
ZBTB12 NM_181842.2 -/. - c.-45297G>A r.(?) p.(=)


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