Variant #0000615633 (NC_000015.9:g.90196146G>A, NM_198525.2:c.16C>T (KIF7))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.90196146G>A
DNA change (hg38) g.89652915G>A
Published as KIF7(NM_198525.2):c.16C>T (p.Q6*)
ISCN -
DB-ID KIF7_000152
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-07 09:38:02 +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.*25829G>A r.(=) p.(=)
KIF7 NM_198525.2 +/. - c.16C>T r.(?) p.(Gln6Ter)


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