Variant #0001005789 (NC_000021.8:g.45971256A>G, NC_000021.8(NM_144991.2):c.303+16413T>C (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.45971256A>G
DNA change (hg38) -
Published as KRTAP10-2(NM_198693.2):c.86T>C (p.(Leu29Pro))
ISCN -
DB-ID TSPEAR_000061
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
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.303+16413T>C r.(=) p.(=)
KRTAP12-2 NM_181684.2 -?/. - c.*115107T>C r.(=) p.(=)
KRTAP12-1 NM_181686.1 -?/. - c.*130492T>C r.(=) p.(=)
KRTAP10-10 NM_181688.1 -?/. - c.-86079A>G r.(?) p.(=)
KRTAP10-4 NM_198687.1 -?/. - c.-22380A>G r.(?) p.(=)
KRTAP10-6 NM_198688.2 -?/. - c.*40012T>C r.(=) p.(=)
KRTAP10-7 NM_198689.2 -?/. - c.-49266A>G r.(?) p.(=)
KRTAP10-9 NM_198690.2 -?/. - c.-75833A>G r.(?) p.(=)
KRTAP10-1 NM_198691.2 -?/. - c.-11223T>C r.(?) p.(=)
KRTAP10-11 NM_198692.2 -?/. - c.-95120A>G r.(?) p.(=)
KRTAP10-2 NM_198693.2 -?/. - c.86T>C r.(?) p.(Leu29Pro)
KRTAP10-5 NM_198694.2 -?/. - c.*28384T>C r.(=) p.(=)
KRTAP10-8 NM_198695.2 -?/. - c.-60762A>G r.(?) p.(=)
KRTAP10-3 NM_198696.2 -?/. - c.*6677T>C r.(=) p.(=)
KRTAP12-3 NM_198697.2 -?/. - c.-106641A>G r.(?) p.(=)
KRTAP12-4 NM_198698.1 -?/. - c.*102937T>C r.(=) p.(=)
KRTAP10-12 NM_198699.1 -?/. - c.-145861A>G r.(?) p.(=)


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