Variant #0000615977 (NC_000016.9:g.3712106C>A, NM_016292.2:c.1822G>T (TRAP1))

Chromosome 16
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.3712106C>A
DNA change (hg38) g.3662105C>A
Published as TRAP1(NM_016292.2):c.1822G>T (p.A608S)
ISCN -
DB-ID DNASE1_000031
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) 0.00012 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNASE1 NM_005223.3 ?/. - c.*4152C>A r.(=) p.(=)
TRAP1 NM_016292.2 ?/. - c.1822G>T r.(?) p.(Ala608Ser)


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