Variant #0000614520 (NC_000013.10:g.21729290_21729291insAGTTTTCTTTGT, NC_000013.10(NM_145061.5):c.1239-2_1239-1insACAAAGAAAACT (SKA3))

Chromosome 13
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.21729290_21729291insAGTTTTCTTTGT
DNA change (hg38) g.21155151_21155152insAGTTTTCTTTGT
Published as SKA3(NM_001166017.1):c.1120-2_1120-1insACAAAGAAAACT (p.?)
ISCN -
DB-ID MRP63_000016
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-03 14:08:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRP63 NM_024026.4 -?/. - c.-21572_-21571insAGTTTTCTTTGT r.(?) p.(=)
SKA3 NM_145061.5 -?/. - c.1239-2_1239-1insACAAAGAAAACT r.spl? p.?


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