Variant #0000570818 (NC_000021.8:g.45949803G>A, NM_144991.2:c.668C>T (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.45949803G>A
DNA change (hg38) g.44529920G>A
Published as TSPEAR(NM_001272037.1):c.464C>T (p.S155L), TSPEAR(NM_144991.2):c.668C>T (p.(Ser223Leu))
ISCN -
DB-ID TSPEAR_000021 See all 2 reported entries
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) 0.00077 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 2024-08-28 13:16:32 +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.668C>T r.(?) p.(Ser223Leu)
KRTAP12-2 NM_181684.2 ?/. - c.*136560C>T r.(=) p.(=)
KRTAP12-1 NM_181686.1 ?/. - c.*151945C>T r.(=) p.(=)
KRTAP10-10 NM_181688.1 ?/. - c.-107532G>A r.(?) p.(=)
KRTAP10-4 NM_198687.1 ?/. - c.-43833G>A r.(?) p.(=)
KRTAP10-6 NM_198688.2 ?/. - c.*61465C>T r.(=) p.(=)
KRTAP10-7 NM_198689.2 ?/. - c.-70719G>A r.(?) p.(=)
KRTAP10-9 NM_198690.2 ?/. - c.-97286G>A r.(?) p.(=)
KRTAP10-1 NM_198691.2 ?/. - c.*9382C>T r.(=) p.(=)
KRTAP10-11 NM_198692.2 ?/. - c.-116573G>A r.(?) p.(=)
KRTAP10-2 NM_198693.2 ?/. - c.*20771C>T r.(=) p.(=)
KRTAP10-5 NM_198694.2 ?/. - c.*49837C>T r.(=) p.(=)
KRTAP10-8 NM_198695.2 ?/. - c.-82215G>A r.(?) p.(=)
KRTAP10-3 NM_198696.2 ?/. - c.*28130C>T r.(=) p.(=)
KRTAP12-3 NM_198697.2 ?/. - c.-128094G>A r.(?) p.(=)
KRTAP12-4 NM_198698.1 ?/. - c.*124390C>T r.(=) p.(=)
KRTAP10-12 NM_198699.1 ?/. - c.-167314G>A r.(?) p.(=)


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