Variant #0000689692 (NC_000006.11:g.2949209T>G, NM_001195291.1:c.668A>C (SERPINB6))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2949209T>G
DNA change (hg38) -
Published as SERPINB6(NM_001297699.1):c.668A>C (p.Y223S)
ISCN -
DB-ID SERPINB6_000028
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPINB6 NM_001195291.1 ?/. - c.668A>C r.(?) p.(Tyr223Ser)
SERPINB6 NM_004568.5 ?/. - c.668A>C r.(?) p.(Tyr223Ser)


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