Variant #0001003982 (NC_000018.9:g.24128121T>C, NC_000018.9(NM_001136205.2):c.-16+734A>G (KCTD1))

Chromosome 18
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.24128121T>C
DNA change (hg38) -
Published as KCTD1(NM_001142730.2):c.380A>G (p.(Gln127Arg))
ISCN -
DB-ID KCTD1_000016
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     
KCTD1 NM_001136205.2 -?/. - c.-16+734A>G r.(=) p.(=)


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