Variant #0000562630 (NC_000017.10:g.61781105G>A, NM_001003786.2:c.1039C>T (STRADA))

Chromosome 17
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.61781105G>A
DNA change (hg38) g.63703745G>A
Published as STRADA(NM_001003787.3):c.1150C>T (p.R384*)
ISCN -
DB-ID LIMD2_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-14 10:35:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STRADA NM_001003786.2 ?/. - c.1039C>T r.(?) p.(Arg347Ter)
MAP3K3 NM_002401.3 ?/. - c.*9968G>A r.(=) p.(=)
LIMD2 NM_030576.3 ?/. - c.-3764C>T r.(?) p.(=)


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