Variant #0000809023 (NC_000019.9:g.51890641C>T, NM_030657.3:c.57G>A (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.51890641C>T
DNA change (hg38) -
Published as LIM2(NM_030657.3):c.57G>A (p.L19=)
ISCN -
DB-ID LIM2_000014
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) 0.00099 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 2021-09-17 14:40:49 +02:00 (CEST)
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.57G>A r.(?) p.(Leu19=)
LIM2 NM_030657.3 -?/. - c.57G>A r.(?) p.(Leu19=)


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