Variant #0000622712 (NC_000011.9:g.68675796G>A, IGHMBP2(NM_002180.2):c.440G>A)

Chromosome 11
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.68675796G>A
DNA change (hg38) g.68908328G>A
Published as IGHMBP2(NM_002180.3):c.440G>A (p.R147Q)
ISCN -
DB-ID IGHMBP2_000202
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) 6.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGHMBP2 NM_002180.2 ?/. - c.440G>A r.(?) p.(Arg147Gln)
MRPL21 NM_181514.1 ?/. - c.-4518C>T r.(?) p.(=)