Variant #0001043621 (NC_000021.8:g.45919823C>T, NC_000021.8(NM_144991.2):c.1857-4G>A (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.45919823C>T
DNA change (hg38) -
Published as TSPEAR(NM_144991.3):c.1857-4G>A
ISCN -
DB-ID TSPEAR_000067
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 2025-05-05 21:14:00 +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.1857-4G>A r.spl? p.?
KRTAP12-2 NM_181684.2 -?/. - c.*166540G>A r.(=) p.(=)
KRTAP12-1 NM_181686.1 -?/. - c.*181925G>A r.(=) p.(=)
KRTAP10-10 NM_181688.1 -?/. - c.-137512C>T r.(?) p.(=)
KRTAP10-4 NM_198687.1 -?/. - c.-73813C>T r.(?) p.(=)
KRTAP10-6 NM_198688.2 -?/. - c.*91445G>A r.(=) p.(=)
KRTAP10-7 NM_198689.2 -?/. - c.-100699C>T r.(?) p.(=)
KRTAP10-9 NM_198690.2 -?/. - c.-127266C>T r.(?) p.(=)
KRTAP10-1 NM_198691.2 -?/. - c.*39362G>A r.(=) p.(=)
KRTAP10-11 NM_198692.2 -?/. - c.-146553C>T r.(?) p.(=)
KRTAP10-2 NM_198693.2 -?/. - c.*50751G>A r.(=) p.(=)
KRTAP10-5 NM_198694.2 -?/. - c.*79817G>A r.(=) p.(=)
KRTAP10-8 NM_198695.2 -?/. - c.-112195C>T r.(?) p.(=)
KRTAP10-3 NM_198696.2 -?/. - c.*58110G>A r.(=) p.(=)
KRTAP12-3 NM_198697.2 -?/. - c.-158074C>T r.(?) p.(=)
KRTAP12-4 NM_198698.1 -?/. - c.*154370G>A r.(=) p.(=)
KRTAP10-12 NM_198699.1 -?/. - c.-197294C>T r.(?) p.(=)


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