Variant #0000317987 (NC_000021.8:g.45950924G>A, NC_000021.8(NM_144991.2):c.633+2C>T (TSPEAR))

Chromosome 21
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45950924G>A
DNA change (hg38) g.44531041G>A
Published as TSPEAR(NM_001272037.1):c.429+2C>T
ISCN -
DB-ID TSPEAR_000008
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) 9.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSPEAR NM_144991.2 +?/. - c.633+2C>T r.spl? p.?
KRTAP12-2 NM_181684.2 +?/. - c.*135439C>T r.(=) p.(=)
KRTAP12-1 NM_181686.1 +?/. - c.*150824C>T r.(=) p.(=)
KRTAP10-10 NM_181688.1 +?/. - c.-106411G>A r.(?) p.(=)
KRTAP10-4 NM_198687.1 +?/. - c.-42712G>A r.(?) p.(=)
KRTAP10-6 NM_198688.2 +?/. - c.*60344C>T r.(=) p.(=)
KRTAP10-7 NM_198689.2 +?/. - c.-69598G>A r.(?) p.(=)
KRTAP10-9 NM_198690.2 +?/. - c.-96165G>A r.(?) p.(=)
KRTAP10-1 NM_198691.2 +?/. - c.*8261C>T r.(=) p.(=)
KRTAP10-11 NM_198692.2 +?/. - c.-115452G>A r.(?) p.(=)
KRTAP10-2 NM_198693.2 +?/. - c.*19650C>T r.(=) p.(=)
KRTAP10-5 NM_198694.2 +?/. - c.*48716C>T r.(=) p.(=)
KRTAP10-8 NM_198695.2 +?/. - c.-81094G>A r.(?) p.(=)
KRTAP10-3 NM_198696.2 +?/. - c.*27009C>T r.(=) p.(=)
KRTAP12-3 NM_198697.2 +?/. - c.-126973G>A r.(?) p.(=)
KRTAP12-4 NM_198698.1 +?/. - c.*123269C>T r.(=) p.(=)
KRTAP10-12 NM_198699.1 +?/. - c.-166193G>A r.(?) p.(=)


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