Variant #0000248770 (NC_000001.10:g.226026406A>G, NM_014698.2:c.*8234T>C (TMEM63A))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.226026406A>G
DNA change (hg38) g.225838705A>G
Published as EPHX1(NM_000120.4):c.416A>G (p.H139R)
ISCN -
DB-ID EPHX1_000008
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) 0.18699 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.416A>G r.(?) p.(His139Arg)
TMEM63A NM_014698.2 -/. - c.*8234T>C r.(=) p.(=)


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