Variant #0000335241 (NC_000023.10:g.114425889C>T, NC_000023.10(NM_020871.3):c.350-2956G>A (LRCH2))

Chromosome X
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.114425889C>T
DNA change (hg38) g.115191326C>T
Published as LRCH2(NM_001243963.1):c.350-2956G>A (p.(=)), RBMXL3(NM_001145346.1):c.1885C>T (p.R629C)
ISCN -
DB-ID LRCH2_000022 See all 2 reported entries
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) 5.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-09-15 15:50:26 +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.1885C>T r.(?) p.(Arg629Cys)
LRCH2 NM_020871.3 ?/. - c.350-2956G>A r.(=) p.(=)


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