Variant #0000259439 (NC_000020.10:g.32881908T>C, NM_000687.2:c.274A>G (AHCY))

Chromosome 20
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.32881908T>C
DNA change (hg38) g.34294102T>C
Published as AHCY(NM_000687.2):c.274A>G (p.(Ile92Val)), AHCY(NM_001161766.2):c.190A>G (p.I64V), AHCY(NM_001322086.1):c.280A>G (p.I94V)
ISCN -
DB-ID AHCY_000003 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) 0.00341 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AHCY NM_000687.2 -?/. - c.274A>G r.(?) p.(Ile92Val)


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