Variant #0000286029 (NC_000018.9:g.2940583_2940585del, NC_000018.9(NM_014646.2):c.698+20_698+22del (LPIN2))

Chromosome 18
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.2940583_2940585del
DNA change (hg38) g.2940585_2940587del
Published as LPIN2(NM_014646.2):c.698+20_698+22delCTT
ISCN -
DB-ID LPIN2_000022
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LPIN2 NM_014646.2 -?/. - c.698+20_698+22del r.(=) p.(=)


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