Variant #0000277917 (NC_000011.9:g.68673601C>G, IGHMBP2(NM_002180.2):c.151C>G)

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.68673601C>G
DNA change (hg38) g.68906133C>G
Published as IGHMBP2(NM_002180.2):c.151C>G (p.Q51E), IGHMBP2(NM_002180.3):c.151C>G (p.Q51E)
ISCN -
DB-ID IGHMBP2_000089 See all 3 reported entries
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) 0.00609 View details
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.151C>G r.(?) p.(Gln51Glu)
MRPL21 NM_181514.1 -/. - c.-2323G>C r.(?) p.(=)