Variant #0000854767 (NC_000017.10:g.1680466_1680469del, NC_000017.10(NM_002615.5):c.998-15_998-12del (SERPINF1))

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.1680466_1680469del
DNA change (hg38) -
Published as SERPINF1(NM_002615.7):c.998-15_998-12delTCTC
ISCN -
DB-ID SERPINF1_000092
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 15:47:41 +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     
SERPINF1 NM_002615.5 -?/. - c.998-15_998-12del r.(=) p.(=)
SMYD4 NM_052928.2 -?/. - c.*4115_*4118del r.(=) p.(=)


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