Variant #0000570812 (NC_000021.8:g.45924771G>A, NC_000021.8(NM_144991.2):c.1755-7C>T (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.45924771G>A
DNA change (hg38) g.44504888G>A
Published as TSPEAR(NM_001272037.1):c.1551-7C>T
ISCN -
DB-ID TSPEAR_000015
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) 0.0014 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 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.1755-7C>T r.(=) p.(=)
KRTAP12-2 NM_181684.2 -?/. - c.*161592C>T r.(=) p.(=)
KRTAP12-1 NM_181686.1 -?/. - c.*176977C>T r.(=) p.(=)
KRTAP10-10 NM_181688.1 -?/. - c.-132564G>A r.(?) p.(=)
KRTAP10-4 NM_198687.1 -?/. - c.-68865G>A r.(?) p.(=)
KRTAP10-6 NM_198688.2 -?/. - c.*86497C>T r.(=) p.(=)
KRTAP10-7 NM_198689.2 -?/. - c.-95751G>A r.(?) p.(=)
KRTAP10-9 NM_198690.2 -?/. - c.-122318G>A r.(?) p.(=)
KRTAP10-1 NM_198691.2 -?/. - c.*34414C>T r.(=) p.(=)
KRTAP10-11 NM_198692.2 -?/. - c.-141605G>A r.(?) p.(=)
KRTAP10-2 NM_198693.2 -?/. - c.*45803C>T r.(=) p.(=)
KRTAP10-5 NM_198694.2 -?/. - c.*74869C>T r.(=) p.(=)
KRTAP10-8 NM_198695.2 -?/. - c.-107247G>A r.(?) p.(=)
KRTAP10-3 NM_198696.2 -?/. - c.*53162C>T r.(=) p.(=)
KRTAP12-3 NM_198697.2 -?/. - c.-153126G>A r.(?) p.(=)
KRTAP12-4 NM_198698.1 -?/. - c.*149422C>T r.(=) p.(=)
KRTAP10-12 NM_198699.1 -?/. - c.-192346G>A r.(?) p.(=)


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