Variant #0000892417 (NC_000015.9:g.90192985C>T, NM_198525.2:c.516G>A (KIF7))

Chromosome 15
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.90192985C>T
DNA change (hg38) -
Published as KIF7(NM_198525.3):c.516G>A (p.E172=)
ISCN -
DB-ID KIF7_000197
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) 0.00085 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TICRR NM_152259.3 -?/. - c.*22668C>T r.(=) p.(=)
KIF7 NM_198525.2 -?/. - c.516G>A r.(?) p.(Glu172=)


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