Variant #0000570819 (NC_000021.8:g.45950945C>G, NM_144991.2:c.614G>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.45950945C>G
DNA change (hg38) g.44531062C>G
Published as TSPEAR(NM_001272037.1):c.410G>C (p.R137T)
ISCN -
DB-ID TSPEAR_000022
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_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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSPEAR NM_144991.2 ?/. - c.614G>C r.(?) p.(Arg205Thr)
KRTAP12-2 NM_181684.2 ?/. - c.*135418G>C r.(=) p.(=)
KRTAP12-1 NM_181686.1 ?/. - c.*150803G>C r.(=) p.(=)
KRTAP10-10 NM_181688.1 ?/. - c.-106390C>G r.(?) p.(=)
KRTAP10-4 NM_198687.1 ?/. - c.-42691C>G r.(?) p.(=)
KRTAP10-6 NM_198688.2 ?/. - c.*60323G>C r.(=) p.(=)
KRTAP10-7 NM_198689.2 ?/. - c.-69577C>G r.(?) p.(=)
KRTAP10-9 NM_198690.2 ?/. - c.-96144C>G r.(?) p.(=)
KRTAP10-1 NM_198691.2 ?/. - c.*8240G>C r.(=) p.(=)
KRTAP10-11 NM_198692.2 ?/. - c.-115431C>G r.(?) p.(=)
KRTAP10-2 NM_198693.2 ?/. - c.*19629G>C r.(=) p.(=)
KRTAP10-5 NM_198694.2 ?/. - c.*48695G>C r.(=) p.(=)
KRTAP10-8 NM_198695.2 ?/. - c.-81073C>G r.(?) p.(=)
KRTAP10-3 NM_198696.2 ?/. - c.*26988G>C r.(=) p.(=)
KRTAP12-3 NM_198697.2 ?/. - c.-126952C>G r.(?) p.(=)
KRTAP12-4 NM_198698.1 ?/. - c.*123248G>C r.(=) p.(=)
KRTAP10-12 NM_198699.1 ?/. - c.-166172C>G r.(?) p.(=)


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