Variant #0000887152 (NC_000006.11:g.31915151C>A, NM_006929.4:c.-11819C>A (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.31915151C>A
DNA change (hg38) -
Published as CFB(NM_001710.6):c.511C>A (p.P171T)
ISCN -
DB-ID C2_000059
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 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 2022-11-01 13:01:21 +01:00 (CET)
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     
C2 NM_000063.4 ?/. - c.*2017C>A r.(=) p.(=)
CFB NM_001710.5 ?/. - c.511C>A r.(?) p.(Pro171Thr)
NELFE NM_002904.5 ?/. - c.*4927G>T r.(=) p.(=)
SKIV2L NM_006929.4 ?/. - c.-11819C>A r.(?) p.(=)
ZBTB12 NM_181842.2 ?/. - c.-45558G>T r.(?) p.(=)


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