Variant #0000924467 (NC_000006.11:g.31831487_31831507dup, NM_001178044.1:c.1904_1924dup (SLC44A4))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.31831487_31831507dup
DNA change (hg38) -
Published as SLC44A4(NM_001178044.1):c.1904_1924dup (p.(Arg641_Pro642insHisAsnGlySerLeuAspArg))
ISCN -
DB-ID NEU1_000024
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 2023-04-16 21:50:28 +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.-954_-934dup r.(?) p.(=)
SLC44A4 NM_001178044.1 ?/. - c.1904_1924dup r.(?) p.(Arg641_Pro642insHisAsnGlySerLeuAspArg)


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