Variant #0000556120 (NC_000015.9:g.90172778G>C, NM_198525.2:c.3345C>G (KIF7))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.90172778G>C
DNA change (hg38) g.89629547G>C
Published as KIF7(NM_198525.2):c.3345C>G (p.H1115Q, p.(His1115Gln)), KIF7(NM_198525.3):c.3345C>G (p.H1115Q)
ISCN -
DB-ID KIF7_000001 See all 27 reported entries
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) 0.01621 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +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.*2461G>C r.(=) p.(=)
KIF7 NM_198525.2 -/. - c.3345C>G r.(?) p.(His1115Gln)


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