Variant #0000570814 (NC_000021.8:g.45945543G>T, NM_144991.2:c.1329C>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.45945543G>T
DNA change (hg38) g.44525660G>T
Published as TSPEAR(NM_001272037.1):c.1125C>A (p.H375Q)
ISCN -
DB-ID TSPEAR_000017
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSPEAR NM_144991.2 ?/. - c.1329C>A r.(?) p.(His443Gln)
KRTAP12-2 NM_181684.2 ?/. - c.*140820C>A r.(=) p.(=)
KRTAP12-1 NM_181686.1 ?/. - c.*156205C>A r.(=) p.(=)
KRTAP10-10 NM_181688.1 ?/. - c.-111792G>T r.(?) p.(=)
KRTAP10-4 NM_198687.1 ?/. - c.-48093G>T r.(?) p.(=)
KRTAP10-6 NM_198688.2 ?/. - c.*65725C>A r.(=) p.(=)
KRTAP10-7 NM_198689.2 ?/. - c.-74979G>T r.(?) p.(=)
KRTAP10-9 NM_198690.2 ?/. - c.-101546G>T r.(?) p.(=)
KRTAP10-1 NM_198691.2 ?/. - c.*13642C>A r.(=) p.(=)
KRTAP10-11 NM_198692.2 ?/. - c.-120833G>T r.(?) p.(=)
KRTAP10-2 NM_198693.2 ?/. - c.*25031C>A r.(=) p.(=)
KRTAP10-5 NM_198694.2 ?/. - c.*54097C>A r.(=) p.(=)
KRTAP10-8 NM_198695.2 ?/. - c.-86475G>T r.(?) p.(=)
KRTAP10-3 NM_198696.2 ?/. - c.*32390C>A r.(=) p.(=)
KRTAP12-3 NM_198697.2 ?/. - c.-132354G>T r.(?) p.(=)
KRTAP12-4 NM_198698.1 ?/. - c.*128650C>A r.(=) p.(=)
KRTAP10-12 NM_198699.1 ?/. - c.-171574G>T r.(?) p.(=)


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