Variant #0000912453 (NC_000006.11:g.31915584A>C, NM_006929.4:c.-11386A>C (SKIV2L))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.31915584A>C
DNA change (hg38) -
Published as CFB(NM_001710.5):c.724A>C (p.I242L, p.(Ile242Leu)), CFB(NM_001710.6):c.724A>C (p.I242L)
ISCN -
DB-ID C2_000018 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) 0.00097 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C2 NM_000063.4 ?/. - c.*2450A>C r.(=) p.(=)
CFB NM_001710.5 ?/. - c.724A>C r.(?) p.(Ile242Leu)
NELFE NM_002904.5 ?/. - c.*4494T>G r.(=) p.(=)
SKIV2L NM_006929.4 ?/. - c.-11386A>C r.(?) p.(=)
ZBTB12 NM_181842.2 ?/. - c.-45991T>G r.(?) p.(=)


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