Variant #0000997195 (NC_000008.10:g.42295041G>A, NM_006749.4:c.989C>T (SLC20A2))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.42295041G>A
DNA change (hg38) -
Published as SLC20A2(NM_001257180.1):c.989C>T (p.(Thr330Ile))
ISCN -
DB-ID C8orf40_000022
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) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC20A2 NM_006749.4 -?/. - c.989C>T r.(?) p.(Thr330Ile)
C8orf40 NM_138436.3 -?/. - c.-101812G>A r.(?) p.(=)


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