Variant #0000528276 (NC_000006.11:g.31828391del, NM_001178044.1:c.*3015del (SLC44A4))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.31828391del
DNA change (hg38) g.31860614del
Published as NEU1(NM_000434.3):c.625del (p.(Glu209Serfs*94))
ISCN -
DB-ID NEU1_000007 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_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 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NEU1 NM_000434.3 +/. - c.625del r.(?) p.(Glu209SerfsTer94)
SLC44A4 NM_001178044.1 +/. - c.*3015del r.(?) p.(=)


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