Variant #0001005424 (NC_000020.10:g.44685026G>A, NM_001134771.1:c.3002G>A (SLC12A5))

Chromosome 20
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.44685026G>A
DNA change (hg38) -
Published as SLC12A5(NM_020708.4):c.2933G>A (p.(Ser978Asn))
ISCN -
DB-ID NCOA5_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC12A5 NM_001134771.1 -?/. - c.3002G>A r.(?) p.(Ser1001Asn)
NCOA5 NM_020967.2 -?/. - c.*5913C>T r.(=) p.(=)


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