Variant #0000505693 (NC_000001.10:g.226016576G>A, NM_014698.2:c.*18064C>T (TMEM63A))

Chromosome 1
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.226016576G>A
DNA change (hg38) g.225828875G>A
Published as EPHX1(NM_001291163.2):c.146G>A (p.R49H)
ISCN -
DB-ID EPHX1_000005
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
EPHX1 NM_000120.3 ?/. - c.146G>A r.(?) p.(Arg49His)
TMEM63A NM_014698.2 ?/. - c.*18064C>T r.(=) p.(=)


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