Variant #0000518611 (NC_000003.11:g.183963255C>A, NC_000003.11(NM_005787.5):c.444+1G>T (ALG3))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.183963255C>A
DNA change (hg38) g.184245467C>A
Published as ALG3(NM_001006941.2):c.300+1G>T
ISCN -
DB-ID ALG3_000016
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) 3.0E-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 2020-06-16 09:21:47 +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.444+1G>T r.spl? p.?
ECE2 NM_014693.3 ?/. - c.-4228C>A r.(?) p.(=)
CAMK2N2 NM_033259.2 ?/. - c.*14690G>T r.(=) p.(=)
VWA5B2 NM_138345.1 ?/. - c.*3429C>A r.(=) p.(=)


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