Variant #0000999215 (NC_000011.9:g.64060642C>T, NM_033310.2:c.152C>T (KCNK4))

Chromosome 11
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.64060642C>T
DNA change (hg38) -
Published as KCNK4(NM_033310.2):c.152C>T (p.(Pro51Leu))
ISCN -
DB-ID BAD_000008
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR137 NM_020155.3 -?/. - c.*3805C>T r.(=) p.(=)
BAD NM_032989.2 -?/. - c.-8548G>A r.(?) p.(=)
KCNK4 NM_033310.2 -?/. - c.152C>T r.(?) p.(Pro51Leu)


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