Variant #0000299507 (NC_000008.10:g.42296993C>T, NM_006749.4:c.909G>A (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.42296993C>T
DNA change (hg38) g.42439475C>T
Published as SLC20A2(NM_001257180.2):c.909G>A (p.A303=), SLC20A2(NM_006749.4):c.909G>A (p.A303=)
ISCN -
DB-ID SLC20A2_000022 See all 2 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) 0.00967 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-23 19:16:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC20A2 NM_006749.4 -?/. - c.909G>A r.(?) p.(Ala303=)
C8orf40 NM_138436.3 -?/. - c.-99860C>T r.(?) p.(=)


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