Variant #0000802488 (NC_000006.11:g.31829178G>A, NM_001178044.1:c.*2226C>T (SLC44A4))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31829178G>A
DNA change (hg38) -
Published as NEU1(NM_000434.3):c.402C>T (p.P134=)
ISCN -
DB-ID NEU1_000019
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) 0.00078 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NEU1 NM_000434.3 -?/. - c.402C>T r.(?) p.(Pro134=)
SLC44A4 NM_001178044.1 -?/. - c.*2226C>T r.(=) p.(=)


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