Variant #0000655035 (NC_000003.11:g.99569473C>T, NM_014890.2:c.327G>A (FILIP1L))

Chromosome 3
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.99569473C>T
DNA change (hg38) g.99850629C>T
Published as FILIP1L(NM_001042459.2):c.1047G>A (p.E349=)
ISCN -
DB-ID CMSS1_000001
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) 5.0E-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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-15 12:29:29 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FILIP1L NM_014890.2 -?/. - c.327G>A r.(?) p.(Glu109=)
CMSS1 NM_032359.3 -?/. - c.64+32586C>T r.(=) p.(=)


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