Variant #0000560715 (NC_000017.10:g.26732301C>T, NM_080669.4:c.414G>A (SLC46A1))

Chromosome 17
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.26732301C>T
DNA change (hg38) g.28405283C>T
Published as SLC46A1(NM_080669.3):c.414G>A (p.Q138=)
ISCN -
DB-ID SLC46A1_000016
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) 0.00015 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SARM1 NM_015077.2 -?/. - c.*8996C>T r.(=) p.(=)
SLC46A1 NM_080669.4 -?/. - c.414G>A r.(?) p.(Gln138=)


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