Variant #0001031756 (NC_000001.10:g.226041445A>G, NM_014698.2:c.1682T>C (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.226041445A>G
DNA change (hg38) -
Published as TMEM63A(NM_014698.3):c.1682T>C (p.I561T)
ISCN -
DB-ID EPHX1_000036
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 2025-05-05 21:14:00 +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.*8397A>G r.(=) p.(=)
TMEM63A NM_014698.2 ?/. - c.1682T>C r.(?) p.(Ile561Thr)


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