Variant #0000990899 (NC_000001.10:g.226034817_226034819del, NM_014698.2:c.2348_2350del (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.226034817_226034819del
DNA change (hg38) -
Published as TMEM63A(NM_014698.2):c.2348_2350delTCA (p.(Ile783del))
ISCN -
DB-ID EPHX1_000028
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 13:07:21 +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.*1769_*1771del r.(=) p.(=)
TMEM63A NM_014698.2 ?/. - c.2348_2350del r.(?) p.(Ile783del)


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