Variant #0000723917 (NC_000012.11:g.125473499G>A, NM_032656.3:c.70C>T (DHX37))

Chromosome 12
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.125473499G>A
DNA change (hg38) -
Published as DHX37(NM_032656.4):c.70C>T (p.P24S)
ISCN -
DB-ID BRI3BP_000010
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DHX37 NM_032656.3 -?/. - c.70C>T r.(?) p.(Pro24Ser)
BRI3BP NM_080626.5 -?/. - c.-4838G>A r.(?) p.(=)


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