Variant #0000271283 (NC_000006.11:g.133789765C>T, NM_004100.4:c.866C>T (EYA4))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.133789765C>T
DNA change (hg38) g.133468627C>T
Published as EYA4(NM_004100.4):c.866C>T (p.T289M), EYA4(NM_004100.5):c.866C>T (p.T289M)
ISCN -
DB-ID EYA4_000016 See all 5 reported entries
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) 0.00066 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EYA4 NM_004100.4 -?/. - c.866C>T r.(?) p.(Thr289Met)


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