Variant #0001042155 (NC_000017.10:g.72745417C>T, NM_004252.4:c.432C>T (SLC9A3R1))

Chromosome 17
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.72745417C>T
DNA change (hg38) -
Published as SLC9A3R1(NM_004252.5):c.432C>T (p.H144=)
ISCN -
DB-ID CD300LF_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) 0.00085 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-05-05 21:14:00 +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     
SLC9A3R1 NM_004252.4 -?/. - c.432C>T r.(?) p.(=)
CD300LF NM_139018.3 -?/. - c.-36412G>A r.(?) p.(=)
RAB37 NM_175738.4 -?/. - c.*3867C>T r.(=) p.(=)


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