Variant #0000320636 (NC_000001.10:g.22902827G>A, NM_020526.3:c.277G>A (EPHA8))

Chromosome 1
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.22902827G>A
DNA change (hg38) g.22576334G>A
Published as EPHA8(NM_001006943.1):c.277G>A (p.(Gly93Ser)), EPHA8(NM_020526.5):c.277G>A (p.G93S)
ISCN -
DB-ID EPHA8_000001 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) 8.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 14:54:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EPHA8 NM_020526.3 ?/. - c.277G>A r.(?) p.(Gly93Ser)


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