Variant #0000821030 (NC_000006.11:g.35782437G>T, NM_182548.3:c.527G>T (LHFPL5))

Chromosome 6
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.35782437G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID LHFPL5_000006 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs774466373
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-11-08 18:28:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LHFPL5 NM_182548.3 ?/. - c.527G>T r.(?) p.(Arg176Leu)


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