Variant #0000605659 (NC_000001.10:g.28293132C>A, NM_001990.3:c.*7845G>T (EYA3))

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.28293132C>A
DNA change (hg38) g.27966621C>A
Published as XKR8(NM_018053.3):c.609C>A (p.Y203*)
ISCN -
DB-ID EYA3_000003
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EYA3 NM_001990.3 ?/. - c.*7845G>T r.(=) p.(=)
XKR8 NM_018053.2 ?/. - c.609C>A r.(?) p.(Tyr203Ter)


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