Variant #0000974379 (NC_000002.11:g.162273024C>A, NM_006593.2:c.103C>A (TBR1))

Chromosome 2
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.162273024C>A
DNA change (hg38) -
Published as TBR1(NM_006593.4):c.103C>A (p.(His35Asn))
ISCN -
DB-ID PSMD14_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 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMD14 NM_005805.5 ?/. - c.*5113C>A r.(=) p.(=)
TBR1 NM_006593.2 ?/. - c.103C>A r.(?) p.(His35Asn)


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