Variant #0000624157 (NC_000020.10:g.39990011C>T, NM_022896.1:c.*2505C>T (LPIN3))

Chromosome 20
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.39990011C>T
DNA change (hg38) g.41361371C>T
Published as EMILIN3(NM_052846.2):c.2198G>A (p.R733H)
ISCN -
DB-ID EMILIN3_000009
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) 4.0E-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 2019-12-06 12:43:26 +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     
LPIN3 NM_022896.1 -?/. - c.*2505C>T r.(=) p.(=)
EMILIN3 NM_052846.1 -?/. - c.2198G>A r.(?) p.(Arg733His)


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