Variant #0000295877 (NC_000015.9:g.65943265C>T, NM_004727.2:c.2778C>T (SLC24A1))

Chromosome 15
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.65943265C>T
DNA change (hg38) g.65650927C>T
Published as SLC24A1(NM_004727.2):c.2778C>T (p.P926=), SLC24A1(NM_004727.3):c.2778C>T (p.P926=)
ISCN -
DB-ID SLC24A1_000026 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) 0.0019 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC24A1 NM_004727.2 -/. - c.2778C>T r.(?) p.(Pro926=)
DENND4A NM_005848.3 -/. - c.*10924G>A r.(=) p.(=)


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