Variant #0000895514 (NC_000021.8:g.46131382_46131391dup, NM_144991.2:c.42_51dup (TSPEAR))

Chromosome 21
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.46131382_46131391dup
DNA change (hg38) -
Published as TSPEAR(NM_144991.3):c.42_51dupGGCCCCCGGC (p.H18Gfs*28)
ISCN -
DB-ID TSPEAR_000055
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSPEAR NM_144991.2 +/. - c.42_51dup r.(?) p.(His18Glyfs*28)
KRTAP12-2 NM_181684.2 +/. - c.-44585_-44576dup r.(?) p.(=)
KRTAP12-1 NM_181686.1 +/. - c.-29350_-29341dup r.(?) p.(=)
KRTAP10-10 NM_181688.1 +/. - c.*73292_*73301dup r.(=) p.(=)
KRTAP10-4 NM_198687.1 +/. - c.*136541_*136550dup r.(=) p.(=)
KRTAP10-6 NM_198688.2 +/. - c.-119023_-119014dup r.(?) p.(=)
KRTAP10-7 NM_198689.2 +/. - c.*109733_*109742dup r.(=) p.(=)
KRTAP10-9 NM_198690.2 +/. - c.*83415_*83424dup r.(=) p.(=)
KRTAP10-1 NM_198691.2 +/. - c.-171355_-171346dup r.(?) p.(=)
KRTAP10-11 NM_198692.2 +/. - c.*64110_*64119dup r.(=) p.(=)
KRTAP10-2 NM_198693.2 +/. - c.-160047_-160038dup r.(?) p.(=)
KRTAP10-5 NM_198694.2 +/. - c.-130933_-130924dup r.(?) p.(=)
KRTAP10-8 NM_198695.2 +/. - c.*98585_*98594dup r.(=) p.(=)
KRTAP10-3 NM_198696.2 +/. - c.-152790_-152781dup r.(?) p.(=)
KRTAP12-3 NM_198697.2 +/. - c.*53195_*53204dup r.(=) p.(=)
KRTAP12-4 NM_198698.1 +/. - c.-56857_-56848dup r.(?) p.(=)
KRTAP10-12 NM_198699.1 +/. - c.*13528_*13537dup r.(=) p.(=)


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