Variant #0000612039 (NC_000009.11:g.140127231T>C, NC_000009.11(NM_080877.2):c.305-5T>C (SLC34A3))

Chromosome 9
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.140127231T>C
DNA change (hg38) g.137232779T>C
Published as SLC34A3(NM_001177316.1):c.305-5T>C (p.?)
ISCN -
DB-ID RNF224_000008
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-26 13:11:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNF224 NM_001190228.1 -?/. - c.*3693T>C r.(=) p.(=)
SLC34A3 NM_080877.2 -?/. - c.305-5T>C r.spl? p.?


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