Variant #0000950813 (NC_000017.10:g.2227572G>A, NM_021947.1:c.*405G>A (SRR))

Chromosome 17
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.2227572G>A
DNA change (hg38) -
Published as TSR1(NM_018128.5):c.2333C>T (p.T778I)
ISCN -
DB-ID SRR_000016
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) 0.002 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-11-27 17:35:39 +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     
TSR1 NM_018128.4 -?/. - c.2333C>T r.(?) p.(Thr778Ile)
SRR NM_021947.1 -?/. - c.*405G>A r.(=) p.(=)


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