Variant #0001004805 (NC_000019.9:g.42503372C>T, NM_152296.4:c.-5144G>A (ATP1A3))

Chromosome 19
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.42503372C>T
DNA change (hg38) -
Published as GRIK5(NM_002088.4):c.2594G>A (p.(Arg865Gln))
ISCN -
DB-ID ATP1A3_000165
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRIK5 NM_002088.4 -?/. - c.2594G>A r.(?) p.(Arg865Gln)
ATP1A3 NM_152296.4 -?/. - c.-5144G>A r.(?) p.(=)


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