Variant #0000536501 (NC_000009.11:g.132576344_132576346del, NM_000113.2:c.907_909del (TOR1A))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.132576344_132576346del
DNA change (hg38) g.129814065_129814067del
Published as TOR1A(NM_000113.3):c.907_909delGAG (p.E303del)
ISCN -
DB-ID TOR1A_000011 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_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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TOR1A NM_000113.2 +/. - c.907_909del r.(?) p.(Glu303del)
TOR1B NM_014506.1 +/. - c.*4482_*4484del r.(=) p.(=)


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