Variant #0000973718 (NC_000001.10:g.226041377G>A, NM_014698.2:c.1750C>T (TMEM63A))

Chromosome 1
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.226041377G>A
DNA change (hg38) -
Published as TMEM63A(NM_014698.3):c.1750C>T (p.(Arg584Cys))
ISCN -
DB-ID EPHX1_000024
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) 0.00096 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 2024-04-19 20:20:39 +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     
EPHX1 NM_000120.3 -?/. - c.*8329G>A r.(=) p.(=)
TMEM63A NM_014698.2 -?/. - c.1750C>T r.(?) p.(Arg584Cys)


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