Variant #0000657634 (NC_000015.9:g.65946296C>T, NM_004727.2:c.3179C>T (SLC24A1))

Chromosome 15
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.65946296C>T
DNA change (hg38) g.65653958C>T
Published as SLC24A1(NM_004727.2):c.3179C>T (p.A1060V)
ISCN -
DB-ID DENND4A_000022
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) 6.0E-5 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 2020-03-23 16:13:27 +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     
SLC24A1 NM_004727.2 ?/. - c.3179C>T r.(?) p.(Ala1060Val)
DENND4A NM_005848.3 ?/. - c.*7893G>A r.(=) p.(=)


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