Variant #0000850354 (NC_000003.11:g.47888493T>G, DHX30(NM_138615.2):c.1929+2T>G)

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.47888493T>G
DNA change (hg38) -
Published as DHX30(NM_138615.3):c.1929+2T>G
ISCN -
DB-ID DHX30_000033
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) Variant not found in online data sets
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP4 NM_002375.4 ?/. - c.*6029A>C r.(=) p.(=)
DHX30 NM_138615.2 ?/. - c.1929+2T>G r.spl? p.?