Variant #0000347485 (NC_000014.8:g.50088697G>C, NM_001083908.1:c.*3563C>G (DNAAF2))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.50088697G>C
DNA change (hg38) g.49621979G>C
Published as -
ISCN -
DB-ID MGAT2_000004 See all 2 reported entries
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL36AL NM_001001.3 +?/. - c.-1454C>G r.(?) p.(=)
DNAAF2 NM_001083908.1 +?/. - c.*3563C>G r.(=) p.(=)
MGAT2 NM_002408.3 +?/. - c.711G>C r.(?) p.(Lys237Asn)


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