Variant #0000542652 (NC_000011.9:g.119077145G>T, NM_005188.3:c.18G>T (CBL))

Chromosome 11
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.119077145G>T
DNA change (hg38) g.119206435G>T
Published as CBL(NM_005188.4):c.18G>T (p.K6N)
ISCN -
DB-ID CBL_000043
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
CCDC153 NM_001145018.1 ?/. - c.-10649C>A r.(?) p.(=)
CBL NM_005188.3 ?/. - c.18G>T r.(?) p.(Lys6Asn)


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