Variant #0000333287 (NC_000023.10:g.17394182_17394217dup, NM_198270.2:c.302_337dup (NHS))

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.17394182_17394217dup
DNA change (hg38) g.17376059_17376094dup
Published as NHS(NM_198270.2):c.302_337dupAGGCGGCGCCCGCAGCCGGCGAGGCGTCCTCGGCGG (p.(Glu101_Ala112dup))
ISCN -
DB-ID NHS_000020
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 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NHS NM_198270.2 -?/. - c.302_337dup r.(?) p.(Glu101_Ala112dup)


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