Variant #0000914345 (NC_000015.9:g.65952598T>C, NM_004727.2:c.*6181T>C (SLC24A1))

Chromosome 15
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.65952598T>C
DNA change (hg38) -
Published as SLC24A1(NM_001301033.2):c.2997-19T>C
ISCN -
DB-ID DENND4A_000034
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-01-11 15:44:22 +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.*6181T>C r.(=) p.(=)
DENND4A NM_005848.3 -?/. - c.*1591A>G r.(=) p.(=)


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