Variant #0000890555 (NC_000012.11:g.39716500G>C, NM_001173464.1:c.3641C>G (KIF21A))

Chromosome 12
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.39716500G>C
DNA change (hg38) -
Published as KIF21A(NM_001173464.1):c.3641C>G (p.P1214R), KIF21A(NM_017641.4):c.3602C>G (p.P1201R)
ISCN -
DB-ID KIF21A_000013 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) 0.00086 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIF21A NM_001173464.1 -?/. - c.3641C>G r.(?) p.(Pro1214Arg)


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