Variant #0000524610 (NC_000005.9:g.14143868G>A, NM_007118.2:c.34G>A (TRIO))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.14143868G>A
DNA change (hg38) g.14143759G>A
Published as TRIO(NM_007118.2):c.34G>A (p.(Ala12Thr)), TRIO(NM_007118.4):c.34G>A (p.A12T)
ISCN -
DB-ID TRIO_000051 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
TRIO NM_007118.2 -?/. - c.34G>A r.(?) p.(Ala12Thr)


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