Variant #0000977846 (NC_000007.13:g.74212260del, NM_173537.2:c.1593del (GTF2IRD2))

Chromosome 7
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.74212260del
DNA change (hg38) -
Published as GTF2IRD2(NM_173537.5):c.1593del (p.(Asn532Thrfs*26))
ISCN -
DB-ID GTF2IRD2_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
GTF2IRD2 NM_173537.2 ?/. - c.1593del r.(?) p.(Asn532Thrfs*26)


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