Variant #0000931227 (NC_000021.8:g.45948383T>C, NM_144991.2:c.874A>G (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.45948383T>C
DNA change (hg38) -
Published as TSPEAR(NM_144991.3):c.874A>G (p.K292E)
ISCN -
DB-ID TSPEAR_000056
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSPEAR NM_144991.2 ?/. - c.874A>G r.(?) p.(Lys292Glu)
KRTAP12-2 NM_181684.2 ?/. - c.*137980A>G r.(=) p.(=)
KRTAP12-1 NM_181686.1 ?/. - c.*153365A>G r.(=) p.(=)
KRTAP10-10 NM_181688.1 ?/. - c.-108952T>C r.(?) p.(=)
KRTAP10-4 NM_198687.1 ?/. - c.-45253T>C r.(?) p.(=)
KRTAP10-6 NM_198688.2 ?/. - c.*62885A>G r.(=) p.(=)
KRTAP10-7 NM_198689.2 ?/. - c.-72139T>C r.(?) p.(=)
KRTAP10-9 NM_198690.2 ?/. - c.-98706T>C r.(?) p.(=)
KRTAP10-1 NM_198691.2 ?/. - c.*10802A>G r.(=) p.(=)
KRTAP10-11 NM_198692.2 ?/. - c.-117993T>C r.(?) p.(=)
KRTAP10-2 NM_198693.2 ?/. - c.*22191A>G r.(=) p.(=)
KRTAP10-5 NM_198694.2 ?/. - c.*51257A>G r.(=) p.(=)
KRTAP10-8 NM_198695.2 ?/. - c.-83635T>C r.(?) p.(=)
KRTAP10-3 NM_198696.2 ?/. - c.*29550A>G r.(=) p.(=)
KRTAP12-3 NM_198697.2 ?/. - c.-129514T>C r.(?) p.(=)
KRTAP12-4 NM_198698.1 ?/. - c.*125810A>G r.(=) p.(=)
KRTAP10-12 NM_198699.1 ?/. - c.-168734T>C r.(?) p.(=)


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