Variant #0001014137 (NC_000005.9:g.492241_492272del, NC_000005.9(NM_004174.2):c.212-43_212-12del (SLC9A3))

Chromosome 5
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.492241_492272del
DNA change (hg38) -
Published as SLC9A3(NM_004174.4):c.212-43_212-12delCTCCCTCACAGCCCGGCCCTGACCTCCCTCCC
ISCN -
DB-ID SLC9A3_000017
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 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC9A3 NM_004174.2 -?/. - c.212-43_212-12del r.(=) p.(=)


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