Variant #0000298118 (NC_000006.11:g.2959513C>T, NM_001195291.1:c.54G>A (SERPINB6))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2959513C>T
DNA change (hg38) g.2959279C>T
Published as SERPINB6(NM_001195291.3):c.66G>A (p.T22=)
ISCN -
DB-ID SERPINB6_000016
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) 0.3485 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
SERPINB6 NM_001195291.1 -/. - c.54G>A r.(?) p.(Thr18=)
SERPINB6 NM_004568.5 -/. - c.54G>A r.(?) p.(Thr18=)


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