Variant #0000852198 (NC_000009.11:g.140127082C>A, NM_080877.2:c.231C>A (SLC34A3))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.140127082C>A
DNA change (hg38) -
Published as SLC34A3(NM_080877.2):c.231C>A (p.C77*)
ISCN -
DB-ID RNF224_000016
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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:40:45 +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     
RNF224 NM_001190228.1 +/. - c.*3544C>A r.(=) p.(=)
SLC34A3 NM_080877.2 +/. - c.231C>A r.(?) p.(Cys77*)


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