Variant #0000335022 (NC_000023.10:g.103495144_103495170dup, NM_153448.3:c.1013_1039dup (ESX1))

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.103495144_103495170dup
DNA change (hg38) g.104250463_104250489dup
Published as ESX1(NM_153448.3):c.1039_1040insGTGTGCCACCCGGGCCGCCCATGGCGC (p.(Arg338_Ala346dup))
ISCN -
DB-ID ESX1_000009
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ESX1 NM_153448.3 -?/. - c.1013_1039dup r.(?) p.(Arg338_Ala346dup)


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