Variant #0000325599 (NC_000017.10:g.72741459G>A, SLC9A3R1(NM_004252.4):c.-3527G>A)

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.72741459G>A
DNA change (hg38) g.74745320G>A
Published as RAB37(NM_001006638.2):c.581G>A (p.(Arg194Gln))
ISCN -
DB-ID RAB37_000004
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) 0.00036 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC9A3R1 NM_004252.4 ?/. - c.-3527G>A r.(?) p.(=)
CD300LF NM_139018.3 ?/. - c.-32454C>T r.(?) p.(=)
RAB37 NM_175738.4 ?/. - c.560G>A r.(?) p.(Arg187Gln)