Variant #0000933359 (NC_000006.11:g.65767506C>T, NC_000006.11(NM_001142800.1):c.2137+1G>A (EYS))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.65767506C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID EYS_000530 See all 10 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs199740930
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00075 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-09-15 08:54:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EYS NM_001142800.1 +/. - c.2137+1G>A r.(?) p.(?)


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