Variant #0000518610 (NC_000003.11:g.183963144T>C, NM_005787.5:c.447A>G (ALG3))

Chromosome 3
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.183963144T>C
DNA change (hg38) g.184245356T>C
Published as ALG3(NM_001006941.2):c.303A>G (p.(=))
ISCN -
DB-ID ALG3_000015
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 09:21:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG3 NM_005787.5 -?/. - c.447A>G r.(?) p.(Val149=)
ECE2 NM_014693.3 -?/. - c.-4339T>C r.(?) p.(=)
CAMK2N2 NM_033259.2 -?/. - c.*14801A>G r.(=) p.(=)
VWA5B2 NM_138345.1 -?/. - c.*3318T>C r.(=) p.(=)


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