Variant #0000610265 (NC_000006.11:g.31828316C>T, NM_001178044.1:c.*3088G>A (SLC44A4))

Chromosome 6
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.31828316C>T
DNA change (hg38) g.31860539C>T
Published as NEU1(NM_000434.3):c.698G>A (p.(Ser233Asn))
ISCN -
DB-ID NEU1_000010
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NEU1 NM_000434.3 +?/. - c.698G>A r.(?) p.(Ser233Asn)
SLC44A4 NM_001178044.1 +?/. - c.*3088G>A r.(=) p.(=)


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