Variant #0000926089 (NC_000015.9:g.90776900C>T, NC_000015.9(NM_006384.3):c.86+1G>A (CIB1))

Chromosome 15
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.90776900C>T
DNA change (hg38) -
Published as CIB1(NM_006384.4):c.86+1G>A
ISCN -
DB-ID CIB1_000009
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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     
GDPGP1 NM_001013657.2 ?/. - c.-766C>T r.(?) p.(=)
TTLL13 NM_001029964.2 ?/. - c.-16152C>T r.(?) p.(=)
NGRN NM_001033088.1 ?/. - c.-32045C>T r.(?) p.(=)
CIB1 NM_006384.3 ?/. - c.86+1G>A r.spl? p.?
SEMA4B NM_198925.2 ?/. - c.*5025C>T r.(=) p.(=)


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