Variant #0000984018 (NC_000021.8:g.46131386G>A, NM_144991.2:c.44C>T (TSPEAR))

Chromosome 21
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.46131386G>A
DNA change (hg38) -
Published as TSPEAR(NM_144991.2):c.44C>T (p.A15V), TSPEAR(NM_144991.3):c.44C>T (p.(Ala15Val))
ISCN -
DB-ID TSPEAR_000035 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) 0.00245 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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.44C>T r.(?) p.(Ala15Val)
KRTAP12-2 NM_181684.2 -?/. - c.-44583C>T r.(?) p.(=)
KRTAP12-1 NM_181686.1 -?/. - c.-29348C>T r.(?) p.(=)
KRTAP10-10 NM_181688.1 -?/. - c.*73296G>A r.(=) p.(=)
KRTAP10-4 NM_198687.1 -?/. - c.*136545G>A r.(=) p.(=)
KRTAP10-6 NM_198688.2 -?/. - c.-119021C>T r.(?) p.(=)
KRTAP10-7 NM_198689.2 -?/. - c.*109737G>A r.(=) p.(=)
KRTAP10-9 NM_198690.2 -?/. - c.*83419G>A r.(=) p.(=)
KRTAP10-1 NM_198691.2 -?/. - c.-171353C>T r.(?) p.(=)
KRTAP10-11 NM_198692.2 -?/. - c.*64114G>A r.(=) p.(=)
KRTAP10-2 NM_198693.2 -?/. - c.-160045C>T r.(?) p.(=)
KRTAP10-5 NM_198694.2 -?/. - c.-130931C>T r.(?) p.(=)
KRTAP10-8 NM_198695.2 -?/. - c.*98589G>A r.(=) p.(=)
KRTAP10-3 NM_198696.2 -?/. - c.-152788C>T r.(?) p.(=)
KRTAP12-3 NM_198697.2 -?/. - c.*53199G>A r.(=) p.(=)
KRTAP12-4 NM_198698.1 -?/. - c.-56855C>T r.(?) p.(=)
KRTAP10-12 NM_198699.1 -?/. - c.*13532G>A r.(=) p.(=)


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