Variant #0000558415 (NC_000016.9:g.5122074_5122077dup, NC_000016.9(NM_019109.4):c.208+16_208+19dup (ALG1))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.5122074_5122077dup
DNA change (hg38) g.5072073_5072076dup
Published as ALG1(NM_019109.5):c.208+15_208+18dupGTCT, ALG1(NM_019109.5):c.208+16_208+19dupTCTG
ISCN -
DB-ID ALG1_000051
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALG1 NM_019109.4 -/. - c.208+16_208+19dup r.(=) p.(=)
FAM86A NM_201400.2 -/. - c.*13557_*13560dup r.(=) p.(=)


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