Variant #0000997384 (NC_000009.11:g.101156471G>T, NM_005458.7:c.1364C>A (GABBR2))

Chromosome 9
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.101156471G>T
DNA change (hg38) -
Published as GABBR2(NM_005458.7):c.1364C>A (p.(Thr455Asn)), GABBR2(NM_005458.8):c.1364C>A (p.T455N)
ISCN -
DB-ID GABBR2_000027 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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
GABBR2 NM_005458.7 ?/. - c.1364C>A r.(?) p.(Thr455Asn)


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