Variant #0001056237 (NC_000017.10:g.79682765_79682766insACAA, NM_012140.4:c.371_372insACAA (SLC25A10))

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.79682765_79682766insACAA
DNA change (hg38) -
Published as SLC25A10(NM_012140.5):c.371_372insACAA (p.(Asn124Lysfs*32))
ISCN -
DB-ID SLC25A10_000006
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 2025-11-01 13:22:20 +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     
SLC25A10 NM_012140.4 ?/. - c.371_372insACAA r.(?) p.(Asn124Lysfs*32)


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