Variant #0000298365 (NC_000017.10:g.72745313C>G, SLC9A3R1(NM_004252.4):c.328C>G)

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.72745313C>G
DNA change (hg38) g.74749174C>G
Published as SLC9A3R1(NM_004252.5):c.328C>G (p.L110V)
ISCN -
DB-ID SLC9A3R1_000002 See all 3 reported entries
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) 0.01469 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.328C>G r.(?) p.(Leu110Val)
CD300LF NM_139018.3 -/. - c.-36308G>C r.(?) p.(=)
RAB37 NM_175738.4 -/. - c.*3763C>G r.(=) p.(=)