Variant #0000573124 (NC_000023.10:g.114427184G>T, NC_000023.10(NM_020871.3):c.350-4251C>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.114427184G>T
DNA change (hg38) g.115192621G>T
Published as RBMXL3(NM_001145346.1):c.3180G>T (p.(Arg1060Ser))
ISCN -
DB-ID LRCH2_000067
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) 1.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.3180G>T r.(?) p.(Arg1060Ser)
LRCH2 NM_020871.3 -?/. - c.350-4251C>A r.(=) p.(=)


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