Variant #0000332175 (NC_000008.10:g.72229909C>T, EYA1(NM_000503.4):c.434G>A)

Chromosome 8
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.72229909C>T
DNA change (hg38) g.71317674C>T
Published as EYA1(NM_000503.4):c.434G>A (p.(Gly145Asp))
ISCN -
DB-ID EYA1_000014
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 View details
Owner VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EYA1 NM_000503.4 ?/. - c.434G>A r.(?) p.(Gly145Asp)