Variant #0000326672 (NC_000019.9:g.48183014_48183015del, NM_015711.3:c.587_588del (GLTSCR1))

Chromosome 19
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.48183014_48183015del
DNA change (hg38) g.47679757_47679758del
Published as GLTSCR1(NM_015711.3):c.586_587del (p.(Pro196LeufsTer477))
ISCN -
DB-ID GLTSCR1_000002
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLTSCR1 NM_015711.3 ?/. - c.587_588del r.(?) p.(Pro196LeufsTer477)


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