Variant #0000624433 (NC_000023.10:g.133607501_133607504del, NC_000023.10(NM_000194.2):c.134+6_134+9del (HPRT1))

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.133607501_133607504del
DNA change (hg38) g.134473471_134473474del
Published as HPRT1(NM_000194.2):c.134+6_134+9delTAAG, HPRT1(NM_000194.3):c.134+6_134+9delTAAG
ISCN -
DB-ID HPRT1_000034 See all 2 reported entries
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HPRT1 NM_000194.2 -?/. - c.134+6_134+9del r.(=) p.(=)


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