Variant #0000998560 (NC_000010.10:g.81470243_81470244insGAGA, NC_000010.10(NR_120613.1):n.757-18431_757-18430insCTCT (NUTM2B-AS1))

Chromosome 10
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.81470243_81470244insGAGA
DNA change (hg38) -
Published as NUTM2B(NM_001278495.1):c.1457_1458insGAGA (p.(His486fs))
ISCN -
DB-ID NUTM2B_000010
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 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)     

Haplotype     

RNA change     

Protein     
NUTM2B NM_001278495.1 ?/. - c.1457_1458insGAGA - r.(?) p.(His486Glnfs*26)
NUTM2B-AS1 NR_120613.1 ?/. - n.757-18431_757-18430insCTCT - r.(?) -


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