Variant #0000560683 (NC_000017.10:g.2238070_2238071del, NM_021947.1:c.*10903_*10904del (SRR))

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.2238070_2238071del
DNA change (hg38) g.2334776_2334777del
Published as TSR1(NM_018128.4):c.676_677delCA (p.Q226Tfs*8)
ISCN -
DB-ID SRR_000009
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-10 18:35:25 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGSM2 NM_014853.2 ?/. - c.-2913_-2912del r.(?) p.(=)
TSR1 NM_018128.4 ?/. - c.676_677del r.(?) p.(Gln226ThrfsTer8)
SRR NM_021947.1 ?/. - c.*10903_*10904del r.(=) p.(=)


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