Variant #0000349476 (NC_000015.9:g.90191827T>C, NM_198525.2:c.1102A>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.90191827T>C
DNA change (hg38) g.89648596T>C
Published as KIF7(NM_198525.2):c.1102A>G (p.T368A), KIF7(NM_198525.3):c.1102A>G (p.T368A)
ISCN -
DB-ID KIF7_000075 See all 5 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) 0.85476 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.*21510T>C r.(=) p.(=)
KIF7 NM_198525.2 -/. - c.1102A>G r.(?) p.(Thr368Ala)


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