Variant #0000613756 (NC_000011.9:g.77727704T>G, NM_023930.3:c.703A>C (KCTD14))

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.77727704T>G
DNA change (hg38) g.78016658T>G
Published as KCTD14(NM_023930.3):c.703A>C (p.(Thr235Pro))
ISCN -
DB-ID KCTD14_000001
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFC2-KCTD14 NM_001203260.1 -?/. - c.*613A>C r.(=) p.(=)
THRSP NM_003251.3 -?/. - c.-47224T>G r.(?) p.(=)
NDUFC2 NM_004549.5 -?/. - c.*53329A>C r.(=) p.(=)
KCTD14 NM_023930.3 -?/. - c.703A>C r.(?) p.(Thr235Pro)


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