Variant #0000534832 (NC_000008.10:g.42275477C>G, NM_006749.4:c.1803G>C (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.42275477C>G
DNA change (hg38) g.42417959C>G
Published as SLC20A2(NM_001257180.2):c.1803G>C (p.S601=)
ISCN -
DB-ID C8orf40_000002
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 19:13:49 +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.1803G>C r.(?) p.(Ser601=)
C8orf40 NM_138436.3 -?/. - c.-121376C>G r.(?) p.(=)


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