Variant #0000950486 (NC_000015.9:g.90774744_90774746del, NC_000015.9(NM_006384.3):c.196-5_196-3del (CIB1))

Chromosome 15
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.90774744_90774746del
DNA change (hg38) -
Published as CIB1(NM_006384.4):c.196-5_196-3delCCT
ISCN -
DB-ID CIB1_000010
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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GDPGP1 NM_001013657.2 -?/. - c.-2922_-2920del r.(?) p.(=)
TTLL13 NM_001029964.2 -?/. - c.-18308_-18306del r.(?) p.(=)
NGRN NM_001033088.1 -?/. - c.-34201_-34199del r.(?) p.(=)
CIB1 NM_006384.3 -?/. - c.196-5_196-3del r.spl? p.?
SEMA4B NM_198925.2 -?/. - c.*2869_*2871del r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.