Variant #0000680631 (NC_000016.9:g.68344265A>C, NM_019023.2:c.-956A>C (PRMT7))

Chromosome 16
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.68344265A>C
DNA change (hg38) -
Published as SLC7A6OS(NM_032178.3):c.444T>G (p.P148=)
ISCN -
DB-ID PRMT7_000007
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC7A6 NM_003983.5 -?/. - c.*13034A>C r.(=) p.(=)
PRMT7 NM_019023.2 -?/. - c.-956A>C r.(?) p.(=)
SLC7A6OS NM_032178.2 -?/. - c.444T>G r.(?) p.(Pro148=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.