Variant #0000615629 (NC_000015.9:g.90191709G>T, NM_198525.2:c.1220C>A (KIF7))

Chromosome 15
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.90191709G>T
DNA change (hg38) g.89648478G>T
Published as KIF7(NM_198525.2):c.1220C>A (p.(Ala407Asp))
ISCN -
DB-ID KIF7_000147
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 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TICRR NM_152259.3 ?/. - c.*21392G>T r.(=) p.(=)
KIF7 NM_198525.2 ?/. - c.1220C>A r.(?) p.(Ala407Asp)


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