Variant #0000991610 (NC_000002.11:g.128398555_128398558del, NM_001136037.2:c.735_738del (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.128398555_128398558del
DNA change (hg38) -
Published as LIMS2(NM_001161403.1):c.669_672delCTGT (p.(Cys224fs))
ISCN -
DB-ID GPR17_000008
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 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYO7B NM_001080527.1 ?/. - c.*3563_*3566del r.(=) p.(=)
LIMS2 NM_001136037.2 ?/. - c.735_738del r.(?) p.(Cys246Profs*39)
GPR17 NM_001161415.1 ?/. - c.-5495_-5492del r.(?) p.(=)


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