Variant #0000951517 (NC_000021.8:g.46011470C>T, NC_000021.8(NM_144991.2):c.83-23581G>A (TSPEAR))

Chromosome 21
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46011470C>T
DNA change (hg38) -
Published as TSPEAR(NM_144991.3):c.83-23581G>A
ISCN -
DB-ID TSPEAR_000058
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 2023-11-27 17:35:39 +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.83-23581G>A r.(=) p.(=)
KRTAP12-2 NM_181684.2 -?/. - c.*74893G>A r.(=) p.(=)
KRTAP12-1 NM_181686.1 -?/. - c.*90278G>A r.(=) p.(=)
KRTAP10-10 NM_181688.1 -?/. - c.-45865C>T r.(?) p.(=)
KRTAP10-4 NM_198687.1 -?/. - c.*16629C>T r.(=) p.(=)
KRTAP10-6 NM_198688.2 -?/. - c.896G>A r.(?) p.(Arg299Lys)
KRTAP10-7 NM_198689.2 -?/. - c.-9052C>T r.(?) p.(=)
KRTAP10-9 NM_198690.2 -?/. - c.-35619C>T r.(?) p.(=)
KRTAP10-1 NM_198691.2 -?/. - c.-51437G>A r.(?) p.(=)
KRTAP10-11 NM_198692.2 -?/. - c.-54906C>T r.(?) p.(=)
KRTAP10-2 NM_198693.2 -?/. - c.-40129G>A r.(?) p.(=)
KRTAP10-5 NM_198694.2 -?/. - c.-11015G>A r.(?) p.(=)
KRTAP10-8 NM_198695.2 -?/. - c.-20548C>T r.(?) p.(=)
KRTAP10-3 NM_198696.2 -?/. - c.-32872G>A r.(?) p.(=)
KRTAP12-3 NM_198697.2 -?/. - c.-66427C>T r.(?) p.(=)
KRTAP12-4 NM_198698.1 -?/. - c.*62723G>A r.(=) p.(=)
KRTAP10-12 NM_198699.1 -?/. - c.-105647C>T r.(?) p.(=)


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