Variant #0000983358 (NC_000019.9:g.33183558T>C, NM_207391.2:c.*15681T>C (RGS9BP))

Chromosome 19
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.33183558T>C
DNA change (hg38) -
Published as NUDT19(NM_001105570.2):c.692T>C (p.(Leu231Ser))
ISCN -
DB-ID ANKRD27_000014
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
NUDT19 NM_001105570.1 ?/. - c.692T>C r.(?) p.(Leu231Ser)
ANKRD27 NM_032139.2 ?/. - c.-17612A>G r.(?) p.(=)
RGS9BP NM_207391.2 ?/. - c.*15681T>C r.(=) p.(=)


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