Variant #0001003038 (NC_000017.10:g.2235661A>G, NM_021947.1:c.*8494A>G (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.2235661A>G
DNA change (hg38) -
Published as TSR1(NM_018128.5):c.1306-8T>C
ISCN -
DB-ID SRR_000031
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) 2.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
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.1306-8T>C r.(=) p.(=)
SRR NM_021947.1 -?/. - c.*8494A>G r.(=) p.(=)


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