Variant #0000290991 (NC_000019.9:g.51883882C>G, NM_030657.3:c.463G>C (LIM2))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.51883882C>G
DNA change (hg38) g.51380628C>G
Published as LIM2(NM_030657.3):c.463G>C (p.V155L)
ISCN -
DB-ID LIM2_000003
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) 0.00022 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LIM2 NM_001161748.1 -?/. - c.337G>C r.(?) p.(Val113Leu)
LIM2 NM_030657.3 -?/. - c.463G>C r.(?) p.(Val155Leu)


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