Variant #0001001793 (NC_000015.9:g.90192407C>A, NM_198525.2:c.721G>T (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.90192407C>A
DNA change (hg38) -
Published as KIF7(NM_198525.2):c.721G>T (p.(Gly241Cys)), KIF7(NM_198525.3):c.721G>T (p.G241C)
ISCN -
DB-ID KIF7_000079 See all 2 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) 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TICRR NM_152259.3 -?/. - c.*22090C>A r.(=) p.(=)
KIF7 NM_198525.2 -?/. - c.721G>T r.(?) p.(Gly241Cys)


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