Variant #0000968698 (NC_000017.10:g.1678467T>C, NM_002615.5:c.759T>C (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.1678467T>C
DNA change (hg38) -
Published as SERPINF1(NM_002615.7):c.759T>C (p.Y253=)
ISCN -
DB-ID SERPINF1_000101
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) 0.0001 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPINF1 NM_002615.5 -?/. - c.759T>C r.(?) p.(=)
SMYD4 NM_052928.2 -?/. - c.*6113A>G r.(=) p.(=)


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