Variant #0001050789 (NC_000002.11:g.128396955G>C, NM_001136037.2:c.993C>G (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.128396955G>C
DNA change (hg38) -
Published as LIMS2(NM_001161403.3):c.927C>G (p.(Tyr309*))
ISCN -
DB-ID GPR17_000010
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
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.*1963G>C r.(=) p.(=)
LIMS2 NM_001136037.2 ?/. - c.993C>G r.(?) p.(Tyr331*)
GPR17 NM_001161415.1 ?/. - c.-7095G>C r.(?) p.(=)


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