Variant #0000997499 (NC_000009.11:g.130592004G>A, NM_000118.3:c.322C>T (ENG))

Chromosome 9
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.130592004G>A
DNA change (hg38) -
Published as ENG(NM_000118.3):c.322C>T (p.H108Y), ENG(NM_001114753.2):c.322C>T (p.(His108Tyr))
ISCN -
DB-ID ENG_000127 See all 3 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) 0.00013 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 2024-08-28 13:16:32 +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     
ENG NM_000118.3 -?/. - c.322C>T r.(?) p.(His108Tyr)


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