Variant #0000515119 (NC_000002.11:g.233659545A>C, KCNJ13(NM_002242.4):c.-18407T>G)

Chromosome 2
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.233659545A>C
DNA change (hg38) g.232794835A>C
Published as GIGYF2(NM_015575.3):c.1370A>C (p.N457T)
ISCN -
DB-ID GIGYF2_000032
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) 0.00039 View details
Owner VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GIGYF2 NM_001103146.1 -?/. - c.1370A>C r.(?) p.(Asn457Thr)
KCNJ13 NM_002242.4 -?/. - c.-18407T>G r.(?) p.(=)