Variant #0000719470 (NC_000003.11:g.47888058_47888059del, NM_138615.2:c.1496_1497del (DHX30))

Chromosome 3
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.47888058_47888059del
DNA change (hg38) -
Published as DHX30(NM_138615.3):c.1496_1497delTG (p.V499Gfs*25)
ISCN -
DB-ID DHX30_000019
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP4 NM_002375.4 ?/. - c.*6465_*6466del r.(=) p.(=)
DHX30 NM_138615.2 ?/. - c.1496_1497del r.(?) p.(Val499Glyfs*25)


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