Variant #0000528029 (NC_000006.11:g.170597400G>A, NM_005618.3:c.597C>T (DLL1))

Chromosome 6
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.170597400G>A
DNA change (hg38) g.170288312G>A
Published as DLL1(NM_005618.3):c.597C>T (p.F199=)
ISCN -
DB-ID DLL1_000002
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) 0.00078 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-22 13:16:37 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DLL1 NM_005618.3 -?/. - c.597C>T r.(?) p.(Phe199=)
FAM120B NM_032448.1 -?/. - c.-18552G>A r.(?) p.(=)


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