Variant #0000334601 (NC_000023.10:g.71131122_71131147dup, NM_001013627.2:c.185_210dup (NHSL2))

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.71131122_71131147dup
DNA change (hg38) g.71911272_71911297dup
Published as NHSL2(NM_001013627.2):c.182_183insGGGGCGCCGCACAGACAGCCTGTACC (p.?)
ISCN -
DB-ID NHSL2_000042
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_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 2020-07-20 15:06:04 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/. - c.185_210dup r.(?) p.(Arg71GlyfsTer32)
RGAG4 NM_001024455.3 ?/. - c.*218083_*218108dup r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.