Variant #0000281720 (NC_000011.9:g.128781978T>G, NM_000890.3:c.810T>G (KCNJ5))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.128781978T>G
DNA change (hg38) g.128912083T>G
Published as KCNJ5(NM_000890.3):c.810T>G (p.L270=), KCNJ5(NM_000890.5):c.810T>G (p.L270=)
ISCN -
DB-ID KCNJ5_000016 See all 4 reported entries
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) 0.83808 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNJ5 NM_000890.3 -/. - c.810T>G r.(?) p.(Leu270=)
C11orf45 NM_145013.2 -/. - c.-6580A>C r.(?) p.(=)


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