Variant #0000727941 (NC_000021.8:g.45924714A>G, NM_144991.2:c.1805T>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.45924714A>G
DNA change (hg38) -
Published as TSPEAR(NM_001272037.1):c.1601T>C (p.V534A)
ISCN -
DB-ID TSPEAR_000046
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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.1805T>C r.(?) p.(Val602Ala)
KRTAP12-2 NM_181684.2 ?/. - c.*161649T>C r.(=) p.(=)
KRTAP12-1 NM_181686.1 ?/. - c.*177034T>C r.(=) p.(=)
KRTAP10-10 NM_181688.1 ?/. - c.-132621A>G r.(?) p.(=)
KRTAP10-4 NM_198687.1 ?/. - c.-68922A>G r.(?) p.(=)
KRTAP10-6 NM_198688.2 ?/. - c.*86554T>C r.(=) p.(=)
KRTAP10-7 NM_198689.2 ?/. - c.-95808A>G r.(?) p.(=)
KRTAP10-9 NM_198690.2 ?/. - c.-122375A>G r.(?) p.(=)
KRTAP10-1 NM_198691.2 ?/. - c.*34471T>C r.(=) p.(=)
KRTAP10-11 NM_198692.2 ?/. - c.-141662A>G r.(?) p.(=)
KRTAP10-2 NM_198693.2 ?/. - c.*45860T>C r.(=) p.(=)
KRTAP10-5 NM_198694.2 ?/. - c.*74926T>C r.(=) p.(=)
KRTAP10-8 NM_198695.2 ?/. - c.-107304A>G r.(?) p.(=)
KRTAP10-3 NM_198696.2 ?/. - c.*53219T>C r.(=) p.(=)
KRTAP12-3 NM_198697.2 ?/. - c.-153183A>G r.(?) p.(=)
KRTAP12-4 NM_198698.1 ?/. - c.*149479T>C r.(=) p.(=)
KRTAP10-12 NM_198699.1 ?/. - c.-192403A>G r.(?) p.(=)


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