Variant #0000249222 (NC_000017.10:g.26727723del, NM_080669.4:c.1224_1226= (SLC46A1))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.26727723del
DNA change (hg38) -
Published as SARM1(NM_015077.4):c.*4419delA, SLC46A1(NM_080669.3):c.1226delT (p.I409Tfs*10)
ISCN -
DB-ID SARM1_000004
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.*4415_*4417= r.(=) p.(=)
SLC46A1 NM_080669.4 -/. - c.1224_1226= r.(=) p.(Gly408=)


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