Variant #0000618912 (NC_000023.10:g.114404882G>T, NM_020871.3:c.978C>A (LRCH2))

Chromosome X
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.114404882G>T
DNA change (hg38) g.115170319G>T
Published as LRCH2(NM_020871.3):c.978C>A (p.P326=)
ISCN -
DB-ID LRCH2_000068
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) Retrieve
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 15:24:38 +01:00 (CET)
Date last edited 2020-07-21 09:00:50 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBMXL3 NM_001145346.1 -?/. - c.-19123G>T r.(?) p.(=)
LRCH2 NM_020871.3 -?/. - c.978C>A r.(?) p.(Pro326=)


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