Variant #0001015527 (NC_000017.10:g.40003655T>C, NM_052935.4:c.-11210A>G (NT5C3B))

Chromosome 17
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.40003655T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID KLHL10_000004
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 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KLHL11 NM_018143.1 ?/. - c.*6337A>G r.(=) p.(=)
NT5C3B NM_052935.4 ?/. - c.-11210A>G r.(?) p.(=)
KLHL10 NM_152467.3 ?/. - c.1445T>C r.(?) p.(Val482Ala)


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