Variant #0000855081 (NC_000017.10:g.72764388T>C, SLC9A3R1(NM_004252.4):c.888+13T>C)

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.72764388T>C
DNA change (hg38) -
Published as SLC9A3R1(NM_004252.5):c.888+13T>C
ISCN -
DB-ID NAT9_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) 0.0014 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 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC9A3R1 NM_004252.4 -?/. - c.888+13T>C r.(=) p.(=)
NAT9 NM_015654.3 -?/. - c.*3475A>G r.(=) p.(=)