Variant #0000302309 (NC_000017.10:g.72744911G>A, SLC9A3R1(NM_004252.4):c.-75G>A)

Chromosome 17
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.72744911G>A
DNA change (hg38) g.74748772G>A
Published as SLC9A3R1(NM_004252.5):c.-75G>A
ISCN -
DB-ID SLC9A3R1_000001
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC9A3R1 NM_004252.4 -/. - c.-75G>A r.(?) p.(=)
CD300LF NM_139018.3 -/. - c.-35906C>T r.(?) p.(=)
RAB37 NM_175738.4 -/. - c.*3361G>A r.(=) p.(=)