Variant #0000560684 (NC_000017.10:g.2238073_2238081del, NM_021947.1:c.*10906_*10914del (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.2238073_2238081del
DNA change (hg38) g.2334779_2334787del
Published as TSR1(NM_018128.4):c.666_674delGTTAGACAC (p.L222_T225delinsF)
ISCN -
DB-ID SRR_000010
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGSM2 NM_014853.2 ?/. - c.-2910_-2902del r.(?) p.(=)
TSR1 NM_018128.4 ?/. - c.666_674del r.(?) p.(Leu222_Thr225delinsPhe)
SRR NM_021947.1 ?/. - c.*10906_*10914del r.(=) p.(=)


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