Variant #0000527238 (NC_000006.11:g.133789883C>A, NC_000006.11(NM_004100.4):c.970+14C>A (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.133789883C>A
DNA change (hg38) g.133468745C>A
Published as EYA4(NM_001301013.1):c.984C>A (p.H328Q), EYA4(NM_001301013.2):c.984C>A (p.H328Q)
ISCN -
DB-ID EYA4_000043 See all 2 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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.970+14C>A r.(=) p.(=)


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