Variant #0000721994 (NC_000008.10:g.42294567_42294568insCA, NM_006749.4:c.1462_1463insTG (SLC20A2))

Chromosome 8
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.42294567_42294568insCA
DNA change (hg38) -
Published as SLC20A2(NM_006749.5):c.1462_1463insTG (p.H488Lfs*21)
ISCN -
DB-ID C8orf40_000015
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC20A2 NM_006749.4 +/. - c.1462_1463insTG r.(?) p.(His488LeufsTer21)
C8orf40 NM_138436.3 +/. - c.-102286_-102285insCA r.(?) p.(=)


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