Variant #0000325103 (NC_000017.10:g.2237942_2237944del, NM_021947.1:c.*10775_*10777del (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.2237942_2237944del
DNA change (hg38) g.2334648_2334650del
Published as TSR1(NM_018128.4):c.806_808del (p.(Val269del)), TSR1(NM_018128.5):c.806_808delTGG (p.V269del)
ISCN -
DB-ID TSR1_000001 See all 2 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +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.-3041_-3039del r.(?) p.(=)
TSR1 NM_018128.4 -?/. - c.806_808del r.(?) p.(Val269del)
SRR NM_021947.1 -?/. - c.*10775_*10777del r.(=) p.(=)


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