Variant #0000616799 (NC_000017.10:g.72348372G>A, NM_153209.3:c.1873G>A (KIF19))

Chromosome 17
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.72348372G>A
DNA change (hg38) g.74352233G>A
Published as KIF19(NM_153209.4):c.1873G>A (p.V625I)
ISCN -
DB-ID BTBD17_000003
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +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     
BTBD17 NM_001080466.1 -?/. - c.*4424C>T r.(=) p.(=)
KIF19 NM_153209.3 -?/. - c.1873G>A r.(?) p.(Val625Ile)


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