Variant #0000576669 (NC_000023.10:g.53627159T>C, NM_031407.5:c.3082A>G (HUWE1))

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.53627159T>C
DNA change (hg38) g.53600199T>C
Published as HUWE1(NM_031407.5):c.3082A>G (p.(Thr1028Ala)), HUWE1(NM_031407.6):c.3082A>G (p.T1028A), HUWE1(NM_031407.7):c.3082A>G (p.T1028A)
ISCN -
DB-ID HUWE1_000048 See all 3 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) 0.00101 View details
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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HUWE1 NM_031407.5 -?/. - c.3082A>G r.(?) p.(Thr1028Ala)


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