Variant #0000518959 (NC_000003.11:g.27763350G>A, NM_005442.2:c.436C>T (EOMES))

Chromosome 3
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.27763350G>A
DNA change (hg38) g.27721859G>A
Published as EOMES(NM_001278182.1):c.436C>T (p.L146F), EOMES(NM_001278182.2):c.436C>T (p.(Leu146Phe))
ISCN -
DB-ID EOMES_000012 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) 0.00086 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 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EOMES NM_005442.2 -?/. - c.436C>T r.(?) p.(Leu146Phe)


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