Variant #0000982375 (NC_000017.10:g.26732203A>T, NM_080669.4:c.512T>A (SLC46A1))

Chromosome 17
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.26732203A>T
DNA change (hg38) -
Published as SLC46A1(NM_080669.3):c.512T>A (p.V171D), SLC46A1(NM_080669.6):c.512T>A (p.(Val171Asp))
ISCN -
DB-ID SLC46A1_000015 See all 3 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) 0.00093 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
SARM1 NM_015077.2 ?/. - c.*8898A>T r.(=) p.(=)
SLC46A1 NM_080669.4 ?/. - c.512T>A r.(?) p.(Val171Asp)


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