Variant #0000945967 (NC_000007.13:g.127670291_127670292delinsTT, NM_022143.4:c.402_403delinsAA (LRRC4))

Chromosome 7
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.127670291_127670292delinsTT
DNA change (hg38) -
Published as -
ISCN -
DB-ID LRRC4_000001
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-11-23 12:44:01 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC4 NM_022143.4 ?/. - c.402_403delinsAA r.(?) p.(Trp134Ter)


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