Variant #0000349070 (NC_000015.9:g.90768918C>T, NM_006384.3:c.*4798G>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.90768918C>T
DNA change (hg38) g.90225686C>T
Published as -
ISCN -
DB-ID SEMA4B_000001
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GDPGP1 NM_001013657.2 ?/. - c.-8748C>T r.(?) p.(=)
TTLL13 NM_001029964.2 ?/. - c.-24134C>T r.(?) p.(=)
NGRN NM_001033088.1 ?/. - c.-40027C>T r.(?) p.(=)
CIB1 NM_006384.3 ?/. - c.*4798G>A r.(=) p.(=)
SEMA4B NM_198925.2 ?/. - c.1547C>T r.(?) p.(Ser516Leu)


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