Variant #0000726243 (NC_000017.10:g.26727715G>C, NM_080669.4:c.1233C>G (SLC46A1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.26727715G>C
DNA change (hg38) -
Published as SLC46A1(NM_080669.3):c.1233C>G (p.N411K)
ISCN -
DB-ID SARM1_000002 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.*4410G>C r.(=) p.(=)
SLC46A1 NM_080669.4 +?/. - c.1233C>G r.(?) p.(Asn411Lys)


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