Variant #0000327504 (NC_000002.11:g.170366919_170366920del, NM_152384.2:c.*5827_*5828del (BBS5))

Chromosome 2
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.170366919_170366920del
DNA change (hg38) g.169510409_169510410del
Published as KLHL41(NM_006063.2):c.631_632del (p.(Arg211GlyfsTer2))
ISCN -
DB-ID KLHL41_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KLHL41 NM_006063.2 ?/. - c.631_632del r.(?) p.(Arg211GlyfsTer2)
BBS5 NM_152384.2 ?/. - c.*5827_*5828del r.(=) p.(=)


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