Variant #0000290292 (NC_000002.11:g.241725798_241725800del, NM_004321.6:c.563_565del (KIF1A))

Chromosome 2
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.241725798_241725800del
DNA change (hg38) g.240786381_240786383del
Published as KIF1A(NM_001244008.1):c.563_565delCCT (p.S188del)
ISCN -
DB-ID KIF1A_000137
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIF1A NM_001244008.1 ?/. - c.563_565del r.(?) p.(Ser188del)
KIF1A NM_004321.6 ?/. - c.563_565del r.(?) p.(Ser188del)


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