Genomic variant #0000332173

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.72184094C>A
DNA change (hg38) -
Published as EYA1(NM_000503.4):c.865G>T (p.(Asp289Tyr), p.(Asp284Tyr), p.(Asp256Tyr))
ISCN -
DB-ID EYA1_000010
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00015 View details
Owner VKGL-NL




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
EYA1 NM_172058.2 -?/. - c.865G>T likely benign r.(?) p.(Asp289Tyr)