Variant #0000509160 (NC_000002.11:g.128431256_128431257dup, NM_001136037.2:c.73_74dup (LIMS2))

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.128431256_128431257dup
DNA change (hg38) g.127673682_127673683dup
Published as LIMS2(NM_001136037.3):c.73_74dupTG (p.W25Cfs*90)
ISCN -
DB-ID GPR17_000005
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LIMS2 NM_001136037.2 ?/. - c.73_74dup r.(?) p.(Trp25CysfsTer90)
GPR17 NM_001161415.1 ?/. - c.*21927_*21928dup r.(=) p.(=)


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