Variant #0000851927 (NC_000008.10:g.42329781_42329793del, NM_006749.4:c.118_130del (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.42329781_42329793del
DNA change (hg38) -
Published as SLC20A2(NM_006749.5):c.118_130delGGTGTGGTGACCT (p.G40*)
ISCN -
DB-ID C8orf40_000020 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +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.118_130del r.(?) p.(Gly40*)
C8orf40 NM_138436.3 +/. - c.-67072_-67060del r.(?) p.(=)


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