Variant #0000557496 (NC_000016.9:g.2230812G>A, NM_032271.2:c.*4237G>A (TRAF7))

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.2230812G>A
DNA change (hg38) g.2180811G>A
Published as CASKIN1(NM_020764.3):c.2557C>T (p.(Pro853Ser))
ISCN -
DB-ID CASKIN1_000010
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) 0.02203 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
CASKIN1 NM_020764.3 -?/. - c.2557C>T r.(?) p.(Pro853Ser)
TRAF7 NM_032271.2 -?/. - c.*4237G>A r.(=) p.(=)


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