Variant #0000930710 (NC_000017.10:g.2239612G>A, NM_021947.1:c.*12445G>A (SRR))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2239612G>A
DNA change (hg38) -
Published as TSR1(NM_018128.5):c.97+13C>T
ISCN -
DB-ID SRR_000014
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) 0.00415 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 2023-07-07 10:10:56 +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     
SGSM2 NM_014853.2 -/. - c.-1371G>A r.(?) p.(=)
TSR1 NM_018128.4 -/. - c.97+13C>T r.(=) p.(=)
SRR NM_021947.1 -/. - c.*12445G>A r.(=) p.(=)


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