Variant #0000324527 (NC_000016.9:g.3716025A>T, NM_016292.2:c.1330T>A (TRAP1))

Chromosome 16
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.3716025A>T
DNA change (hg38) g.3666024A>T
Published as TRAP1(NM_001272049.1):c.1171T>A (p.(Tyr391Asn))
ISCN -
DB-ID TRAP1_000001 See all 2 reported entries
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) 0.0045 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNASE1 NM_005223.3 -?/. - c.*8071A>T r.(=) p.(=)
TRAP1 NM_016292.2 -?/. - c.1330T>A r.(?) p.(Tyr444Asn)


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