Variant #0000574243 (NC_000023.10:g.152719991_152720006del, NM_001711.4:c.-40592_-40577del (BGN))

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.152719991_152720006del
DNA change (hg38) g.153454533_153454548del
Published as HAUS7(NM_017518.7):c.961-19_961-4del (p.?)
ISCN -
DB-ID BGN_000040
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BGN NM_001711.4 -?/. - c.-40592_-40577del r.(?) p.(=)
HAUS7 NM_017518.6 -?/. - c.961-19_961-4del r.spl? p.?


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