Variant #0000807232 (NC_000016.9:g.2225387T>A, NM_032271.2:c.1472T>A (TRAF7))

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.2225387T>A
DNA change (hg38) -
Published as TRAF7(NM_032271.3):c.1472T>A (p.V491E)
ISCN -
DB-ID CASKIN1_000019
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) 1.0E-5 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASKIN1 NM_020764.3 ?/. - c.*3164A>T r.(=) p.(=)
TRAF7 NM_032271.2 ?/. - c.1472T>A r.(?) p.(Val491Glu)


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