Variant #0000977628 (NC_000007.13:g.1525062_1525064del, NM_001080453.2:c.3022_3024del (INTS1))

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.1525062_1525064del
DNA change (hg38) -
Published as INTS1(NM_001080453.3):c.3022_3024del (p.(Glu1008del)), INTS1(NM_001080453.3):c.3022_3024delGAG (p.E1008del)
ISCN -
DB-ID INTS1_000050 See all 2 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) 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INTS1 NM_001080453.2 ?/. - c.3022_3024del r.(?) p.(Glu1008del)


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