Variant #0000544838 (NC_000011.9:g.64055923C>T, NM_033310.2:c.-3193C>T (KCNK4))

Chromosome 11
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.64055923C>T
DNA change (hg38) g.64288451C>T
Published as GPR137(NM_001170881.1):c.745C>T (p.R249W)
ISCN -
DB-ID BAD_000004
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR137 NM_020155.3 ?/. - c.895C>T r.(?) p.(Arg299Trp)
BAD NM_032989.2 ?/. - c.-3829G>A r.(?) p.(=)
KCNK4 NM_033310.2 ?/. - c.-3193C>T r.(?) p.(=)


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