Variant #0000515518 (NC_000002.11:g.27282164A>G, NM_021831.5:c.1981A>G (AGBL5))

Chromosome 2
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.27282164A>G
DNA change (hg38) g.27059296A>G
Published as AGBL5(NM_021831.5):c.1981A>G (p.M661V)
ISCN -
DB-ID AGBL5_000034
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) 2.0E-5 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OST4 NM_001134693.1 -?/. - c.*11449T>C r.(=) p.(=)
AGBL5 NM_021831.5 -?/. - c.1981A>G r.(?) p.(Met661Val)


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