Variant #0000546202 (NC_000012.11:g.102147250_102147251del, NM_024312.4:c.3503_3504del (GNPTAB))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.102147250_102147251del
DNA change (hg38) g.101753472_101753473del
Published as GNPTAB(NM_024312.4):c.3503_3504delTC (p.L1168Qfs*5), GNPTAB(NM_024312.5):c.3503_3504delTC (p.L1168Qfs*5)
ISCN -
DB-ID GNPTAB_000001 See all 6 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPTAB NM_024312.4 +?/. - c.3503_3504del r.(?) p.(Leu1168GlnfsTer5)


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