Variant #0000505464 (NC_000001.10:g.220101281_220101283delinsGG, NM_018713.2:c.500_502delinsCC (SLC30A10))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.220101281_220101283delinsGG
DNA change (hg38) g.219927939_219927941delinsGG
Published as SLC30A10(NM_018713.2):c.500_502delTCGinsCC (p.F167Sfs*25)
ISCN -
DB-ID SLC30A10_000018
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC30A10 NM_018713.2 +/. - c.500_502delinsCC r.(?) p.(Phe167SerfsTer25)


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