Variant #0001013195 (NC_000001.10:g.115222237T>A, NM_000036.2:c.959A>T (AMPD1))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.115222237T>A
DNA change (hg38) -
Published as AMPD1(NM_000036.2):c.959A>T (p.K320I), AMPD1(NM_000036.3):c.860A>T (p.K287I)
ISCN -
DB-ID AMPD1_000003 See all 5 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) 0.02882 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 20:49:11 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMPD1 NM_000036.2 -/. - c.959A>T r.(?) p.(Lys320Ile)


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