Variant #0000611619 (NC_000008.10:g.42329771C>T, NM_006749.4:c.138G>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.42329771C>T
DNA change (hg38) g.42472253C>T
Published as SLC20A2(NM_001257180.2):c.138G>A (p.Q46=)
ISCN -
DB-ID SLC20A2_000037 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) 0.00028 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-23 19:18:14 +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.138G>A r.(?) p.(Gln46=)
C8orf40 NM_138436.3 -?/. - c.-67082C>T r.(?) p.(=)


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