Variant #0000569574 (NC_000020.10:g.39984582C>T, NM_022896.1:c.1711C>T (LPIN3))

Chromosome 20
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.39984582C>T
DNA change (hg38) g.41355942C>T
Published as LPIN3(NM_001301860.1):c.1714C>T (p.P572S)
ISCN -
DB-ID EMILIN3_000006
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) 1.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
LPIN3 NM_022896.1 ?/. - c.1711C>T r.(?) p.(Pro571Ser)
EMILIN3 NM_052846.1 ?/. - c.*5326G>A r.(=) p.(=)


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