Variant #0001020224 (NC_000006.11:g.133703528A>G, NC_000006.11(NM_004100.4):c.34-2A>G (EYA4))

Chromosome 6
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.133703528A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID EYA4_000116
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1786297103
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-01-06 09:24:01 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EYA4 NM_004100.4 ?/. - c.34-2A>G r.(?) p.(?)


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