Variant #0001006952 (NC_000023.10:g.73641371_73641376dup, NM_006517.4:c.-102_-97dup (SLC16A2))

Chromosome X
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.73641371_73641376dup
DNA change (hg38) -
Published as SLC16A2(NM_006517.4):c.-102_-97dupGGCAGC (p.?), SLC16A2(NM_006517.5):c.-102_-97dupGGCAGC
ISCN -
DB-ID SLC16A2_000057 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC16A2 NM_006517.4 -?/. - c.-102_-97dup r.(?) p.(=)


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