Variant #0000862005 (NC_000010.10:g.81466121G>A, NC_000010.10(NR_120613.1):n.757-14309C>T (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.81466121G>A
DNA change (hg38) -
Published as NUTM2B(NM_001278495.1):c.706G>A (p.A236T)
ISCN -
DB-ID NUTM2B_000006
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
NUTM2B NM_001278495.1 ?/. - c.706G>A - r.(?) p.(Ala236Thr)
NUTM2B-AS1 NR_120613.1 ?/. - n.757-14309C>T - r.(?) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.