Variant #0000863081 (NC_000012.11:g.57944106C>T, NM_004984.2:c.52C>T (KIF5A))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.57944106C>T
DNA change (hg38) -
Published as KIF5A(NM_004984.4):c.52C>T (p.P18S)
ISCN -
DB-ID DCTN2_000004 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 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 2022-05-09 15:51:19 +02:00 (CEST)
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     
KIF5A NM_004984.2 ?/. - c.52C>T r.(?) p.(Pro18Ser)
DCTN2 NM_006400.4 ?/. - c.-3260G>A r.(?) p.(=)
MBD6 NM_052897.3 ?/. - c.*21089C>T r.(=) p.(=)


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