Variant #0000279091 (NC_000002.11:g.128400583G>A, NM_001136037.2:c.490C>T (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.128400583G>A
DNA change (hg38) g.127643008G>A
Published as LIMS2(NM_001161404.2):c.409C>T (p.R137W)
ISCN -
DB-ID LIMS2_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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
LIMS2 NM_001136037.2 ?/. - c.490C>T r.(?) p.(Arg164Trp)
GPR17 NM_001161415.1 ?/. - c.-3467G>A r.(?) p.(=)


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