Variant #0001043622 (NC_000021.8:g.45929263C>G, NM_144991.2:c.1573G>C (TSPEAR))

Chromosome 21
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45929263C>G
DNA change (hg38) -
Published as TSPEAR(NM_144991.3):c.1573G>C (p.(Gly525Arg))
ISCN -
DB-ID TSPEAR_000068
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) 3.0E-5 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 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.1573G>C r.(?) p.(Gly525Arg)
KRTAP12-2 NM_181684.2 ?/. - c.*157100G>C r.(=) p.(=)
KRTAP12-1 NM_181686.1 ?/. - c.*172485G>C r.(=) p.(=)
KRTAP10-10 NM_181688.1 ?/. - c.-128072C>G r.(?) p.(=)
KRTAP10-4 NM_198687.1 ?/. - c.-64373C>G r.(?) p.(=)
KRTAP10-6 NM_198688.2 ?/. - c.*82005G>C r.(=) p.(=)
KRTAP10-7 NM_198689.2 ?/. - c.-91259C>G r.(?) p.(=)
KRTAP10-9 NM_198690.2 ?/. - c.-117826C>G r.(?) p.(=)
KRTAP10-1 NM_198691.2 ?/. - c.*29922G>C r.(=) p.(=)
KRTAP10-11 NM_198692.2 ?/. - c.-137113C>G r.(?) p.(=)
KRTAP10-2 NM_198693.2 ?/. - c.*41311G>C r.(=) p.(=)
KRTAP10-5 NM_198694.2 ?/. - c.*70377G>C r.(=) p.(=)
KRTAP10-8 NM_198695.2 ?/. - c.-102755C>G r.(?) p.(=)
KRTAP10-3 NM_198696.2 ?/. - c.*48670G>C r.(=) p.(=)
KRTAP12-3 NM_198697.2 ?/. - c.-148634C>G r.(?) p.(=)
KRTAP12-4 NM_198698.1 ?/. - c.*144930G>C r.(=) p.(=)
KRTAP10-12 NM_198699.1 ?/. - c.-187854C>G r.(?) p.(=)
TSPEAR-AS1 NR_103707.1 ?/. - n.1343C>G r.(?) -


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