Variant #0001006620 (NC_000023.10:g.17737463_17737465dup, NC_000023.10(NM_198270.2):c.853-2098_853-2096dup (NHS))

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.17737463_17737465dup
DNA change (hg38) -
Published as NHS(NM_001136024.2):c.322-1_323dupGTT (p.(Thr107_Phe108insLeu))
ISCN -
DB-ID NHS_000162
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NHS NM_198270.2 ?/. - c.853-2098_853-2096dup r.(=) p.(=)


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