Variant #0000535550 (NC_000009.11:g.100388125dup, NM_139246.4:c.320dup (TSTD2))

Chromosome 9
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.100388125dup
DNA change (hg38) g.97625843dup
Published as TSTD2(NM_139246.4):c.320dupA (p.(Thr108AspfsTer23))
ISCN -
DB-ID TMOD1_000004
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-25 16:45:47 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NCBP1 NM_002486.4 ?/. - c.-8039dup r.(?) p.(=)
TMOD1 NM_003275.3 ?/. - c.*26145dup r.(?) p.(=)
TSTD2 NM_139246.4 ?/. - c.320dup r.(?) p.(Thr108AspfsTer23)


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