Variant #0000317983 (NC_000021.8:g.45929090G>A, NM_144991.2:c.1746C>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.45929090G>A
DNA change (hg38) g.44509207G>A
Published as TSPEAR(NM_001272037.1):c.1542C>T (p.L514=)
ISCN -
DB-ID TSPEAR_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) 0.00338 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 2020-08-06 14:59:34 +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.1746C>T r.(?) p.(Leu582=)
KRTAP12-2 NM_181684.2 -?/. - c.*157273C>T r.(=) p.(=)
KRTAP12-1 NM_181686.1 -?/. - c.*172658C>T r.(=) p.(=)
KRTAP10-10 NM_181688.1 -?/. - c.-128245G>A r.(?) p.(=)
KRTAP10-4 NM_198687.1 -?/. - c.-64546G>A r.(?) p.(=)
KRTAP10-6 NM_198688.2 -?/. - c.*82178C>T r.(=) p.(=)
KRTAP10-7 NM_198689.2 -?/. - c.-91432G>A r.(?) p.(=)
KRTAP10-9 NM_198690.2 -?/. - c.-117999G>A r.(?) p.(=)
KRTAP10-1 NM_198691.2 -?/. - c.*30095C>T r.(=) p.(=)
KRTAP10-11 NM_198692.2 -?/. - c.-137286G>A r.(?) p.(=)
KRTAP10-2 NM_198693.2 -?/. - c.*41484C>T r.(=) p.(=)
KRTAP10-5 NM_198694.2 -?/. - c.*70550C>T r.(=) p.(=)
KRTAP10-8 NM_198695.2 -?/. - c.-102928G>A r.(?) p.(=)
KRTAP10-3 NM_198696.2 -?/. - c.*48843C>T r.(=) p.(=)
KRTAP12-3 NM_198697.2 -?/. - c.-148807G>A r.(?) p.(=)
KRTAP12-4 NM_198698.1 -?/. - c.*145103C>T r.(=) p.(=)
KRTAP10-12 NM_198699.1 -?/. - c.-188027G>A r.(?) p.(=)
TSPEAR-AS1 NR_103707.1 -?/. - n.1215-45G>A r.(?) -


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