Variant #0000658226 (NC_000017.10:g.61781104C>T, NM_001003786.2:c.1040G>A (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.61781104C>T
DNA change (hg38) g.63703744C>T
Published as STRADA(NM_001003787.3):c.1151G>A (p.R384Q)
ISCN -
DB-ID LIMD2_000003
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) 3.0E-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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STRADA NM_001003786.2 ?/. - c.1040G>A r.(?) p.(Arg347Gln)
MAP3K3 NM_002401.3 ?/. - c.*9967C>T r.(=) p.(=)
LIMD2 NM_030576.3 ?/. - c.-3763G>A r.(?) p.(=)


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