Variant #0000676605 (NC_000002.11:g.27281318G>A, NM_021831.5:c.1722G>A (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.27281318G>A
DNA change (hg38) -
Published as AGBL5(NM_021831.5):c.1722G>A (p.P574=)
ISCN -
DB-ID AGBL5_000040
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) 4.0E-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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OST4 NM_001134693.1 -?/. - c.*12295C>T r.(=) p.(=)
AGBL5 NM_021831.5 -?/. - c.1722G>A r.(?) p.(Pro574=)


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