Variant #0000545532 (NC_000011.9:g.68675806G>C, IGHMBP2(NM_002180.2):c.449+1G>C)

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.68675806G>C
DNA change (hg38) g.68908338G>C
Published as IGHMBP2(NM_002180.3):c.449+1G>C
ISCN -
DB-ID IGHMBP2_000177
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGHMBP2 NM_002180.2 ?/. - c.449+1G>C r.spl? p.?
MRPL21 NM_181514.1 ?/. - c.-4528C>G r.(?) p.(=)