Variant #0001027346 (NC_000021.8:g.45951009C>T, NM_144991.2:c.550G>A (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.45951009C>T
DNA change (hg38) -
Published as TSPEAR(NM_144991.3):c.550G>A (p.D184N)
ISCN -
DB-ID TSPEAR_000066
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
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.550G>A r.(?) p.(Asp184Asn)
KRTAP12-2 NM_181684.2 ?/. - c.*135354G>A r.(=) p.(=)
KRTAP12-1 NM_181686.1 ?/. - c.*150739G>A r.(=) p.(=)
KRTAP10-10 NM_181688.1 ?/. - c.-106326C>T r.(?) p.(=)
KRTAP10-4 NM_198687.1 ?/. - c.-42627C>T r.(?) p.(=)
KRTAP10-6 NM_198688.2 ?/. - c.*60259G>A r.(=) p.(=)
KRTAP10-7 NM_198689.2 ?/. - c.-69513C>T r.(?) p.(=)
KRTAP10-9 NM_198690.2 ?/. - c.-96080C>T r.(?) p.(=)
KRTAP10-1 NM_198691.2 ?/. - c.*8176G>A r.(=) p.(=)
KRTAP10-11 NM_198692.2 ?/. - c.-115367C>T r.(?) p.(=)
KRTAP10-2 NM_198693.2 ?/. - c.*19565G>A r.(=) p.(=)
KRTAP10-5 NM_198694.2 ?/. - c.*48631G>A r.(=) p.(=)
KRTAP10-8 NM_198695.2 ?/. - c.-81009C>T r.(?) p.(=)
KRTAP10-3 NM_198696.2 ?/. - c.*26924G>A r.(=) p.(=)
KRTAP12-3 NM_198697.2 ?/. - c.-126888C>T r.(?) p.(=)
KRTAP12-4 NM_198698.1 ?/. - c.*123184G>A r.(=) p.(=)
KRTAP10-12 NM_198699.1 ?/. - c.-166108C>T r.(?) p.(=)


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