Variant #0000290062 (NC_000002.11:g.233633157T>G, KCNJ13(NM_002242.4):c.827A>C)

Chromosome 2
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.233633157T>G
DNA change (hg38) g.232768447T>G
Published as KCNJ13(NM_002242.4):c.827A>C (p.E276A)
ISCN -
DB-ID KCNJ13_000007 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00037 View details
Owner VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GIGYF2 NM_001103146.1 ?/. - c.532+7011T>G r.(=) p.(=)
KCNJ13 NM_002242.4 ?/. - c.827A>C r.(?) p.(Glu276Ala)