Variant #0000254199 (NC_000002.11:g.233712227A>G, NM_002242.4:c.-71089T>C (KCNJ13))

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.233712227A>G
DNA change (hg38) g.232847517A>G
Published as GIGYF2(NM_001103147.1):c.3693A>G (p.P1231=)
ISCN -
DB-ID GIGYF2_000021
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GIGYF2 NM_001103146.1 -?/. - c.3630A>G r.(?) p.(Pro1210=)
KCNJ13 NM_002242.4 -?/. - c.-71089T>C r.(?) p.(=)


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