Variant #0000606073 (NC_000002.11:g.11932055A>G, NM_145693.2:c.1621A>G (LPIN1))

Chromosome 2
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.11932055A>G
DNA change (hg38) g.11791929A>G
Published as LPIN1(NM_001261428.2):c.1876A>G (p.I626V)
ISCN -
DB-ID LPIN1_000028
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) 0.00219 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LPIN1 NM_001261428.1 -?/. - c.1876A>G r.(?) p.(Ile626Val)
LPIN1 NM_145693.2 -?/. - c.1621A>G r.(?) p.(Ile541Val)


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