Variant #0000656314 (NC_000009.11:g.140127051G>A, NM_080877.2:c.200G>A (SLC34A3))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140127051G>A
DNA change (hg38) g.137232599G>A
Published as SLC34A3(NM_080877.2):c.200G>A (p.R67H)
ISCN -
DB-ID RNF224_000011
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) 0.09877 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNF224 NM_001190228.1 -/. - c.*3513G>A r.(=) p.(=)
SLC34A3 NM_080877.2 -/. - c.200G>A r.(?) p.(Arg67His)


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