Variant #0001025645 (NC_000009.11:g.140123299C>T, NM_080877.2:c.-2272C>T (SLC34A3))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.140123299C>T
DNA change (hg38) -
Published as RNF224(NM_001190228.2):c.232C>T (p.R78C)
ISCN -
DB-ID C9orf169_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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +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.232C>T r.(?) p.(Arg78Cys)
SLC34A3 NM_080877.2 ?/. - c.-2272C>T r.(?) p.(=)
C9orf169 NM_199001.2 ?/. - c.*2791C>T r.(=) p.(=)


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