Variant #0000802490 (NC_000006.11:g.31833288T>C, NM_001178044.1:c.1547A>G (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.31833288T>C
DNA change (hg38) -
Published as SLC44A4(NM_001178045.1):c.1445A>G (p.N482S)
ISCN -
DB-ID NEU1_000021
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) 0.00016 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.-2735A>G r.(?) p.(=)
SLC44A4 NM_001178044.1 ?/. - c.1547A>G r.(?) p.(Asn516Ser)


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