Variant #0000968727 (NC_000017.10:g.18907093_18907095inv, NC_000017.10(NM_152351.4):c.983-9582_983-9580inv (SLC5A10))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.18907093_18907095inv
DNA change (hg38) -
Published as -
ISCN -
DB-ID FAM83G_000010
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-02-26 20:06:56 +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     
FAM83G NM_001039999.2 +?/. - c.260_262inv r.(?) p.(Ser87*)
GRAP NM_006613.3 +?/. - c.*18177_*18179inv r.(=) p.(=)
SLC5A10 NM_152351.4 +?/. - c.983-9582_983-9580inv r.(=) p.(=)


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