Variant #0000996638 (NC_000007.13:g.73457316G>A, NM_000501.2:c.328G>A (ELN))

Chromosome 7
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.73457316G>A
DNA change (hg38) -
Published as ELN(NM_000501.4):c.328G>A (p.A110T), ELN(NM_001278939.1):c.328G>A (p.A110T), ELN(NM_001278939.2):c.328G>A (p.A110T)
ISCN -
DB-ID ELN_000017 See all 4 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) 0.00049 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
ELN NM_000501.2 -?/. - c.328G>A r.(?) p.(Ala110Thr)


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