Variant #0000809912 (NC_000023.10:g.133607438A>C, NM_000194.2:c.77A>C (HPRT1))

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.133607438A>C
DNA change (hg38) -
Published as HPRT1(NM_000194.2):c.77A>C (p.(Asn26Thr)), HPRT1(NM_000194.3):c.77A>C (p.N26T)
ISCN -
DB-ID HPRT1_000010 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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HPRT1 NM_000194.2 ?/. - c.77A>C r.(?) p.(Asn26Thr)


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