Variant #0000809417 (NC_000021.8:g.45947185A>T, NM_144991.2:c.1139T>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.45947185A>T
DNA change (hg38) -
Published as TSPEAR(NM_144991.3):c.1139T>A (p.I380N)
ISCN -
DB-ID TSPEAR_000050
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 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 2021-09-17 14:40:49 +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.1139T>A r.(?) p.(Ile380Asn)
KRTAP12-2 NM_181684.2 ?/. - c.*139178T>A r.(=) p.(=)
KRTAP12-1 NM_181686.1 ?/. - c.*154563T>A r.(=) p.(=)
KRTAP10-10 NM_181688.1 ?/. - c.-110150A>T r.(?) p.(=)
KRTAP10-4 NM_198687.1 ?/. - c.-46451A>T r.(?) p.(=)
KRTAP10-6 NM_198688.2 ?/. - c.*64083T>A r.(=) p.(=)
KRTAP10-7 NM_198689.2 ?/. - c.-73337A>T r.(?) p.(=)
KRTAP10-9 NM_198690.2 ?/. - c.-99904A>T r.(?) p.(=)
KRTAP10-1 NM_198691.2 ?/. - c.*12000T>A r.(=) p.(=)
KRTAP10-11 NM_198692.2 ?/. - c.-119191A>T r.(?) p.(=)
KRTAP10-2 NM_198693.2 ?/. - c.*23389T>A r.(=) p.(=)
KRTAP10-5 NM_198694.2 ?/. - c.*52455T>A r.(=) p.(=)
KRTAP10-8 NM_198695.2 ?/. - c.-84833A>T r.(?) p.(=)
KRTAP10-3 NM_198696.2 ?/. - c.*30748T>A r.(=) p.(=)
KRTAP12-3 NM_198697.2 ?/. - c.-130712A>T r.(?) p.(=)
KRTAP12-4 NM_198698.1 ?/. - c.*127008T>A r.(=) p.(=)
KRTAP10-12 NM_198699.1 ?/. - c.-169932A>T r.(?) p.(=)


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