Variant #0000308032 (NC_000001.10:g.36775182C>T, NM_024676.4:c.427C>T (SH3D21))

Chromosome 1
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.36775182C>T
DNA change (hg38) g.36309581C>T
Published as SH3D21(NM_001162530.2):c.760C>T (p.R254W)
ISCN -
DB-ID SH3D21_000001
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) 4.0E-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 2018-01-15 20:58:59 +01:00 (CET)
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     
THRAP3 NM_005119.3 ?/. - c.*5564C>T r.(=) p.(=)
EVA1B NM_018166.1 ?/. - c.*12714G>A r.(=) p.(=)
SH3D21 NM_024676.4 ?/. - c.427C>T r.(?) p.(Arg143Trp)


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