Variant #0000999423 (NC_000011.9:g.68675621G>A, NM_002180.2:c.265G>A (IGHMBP2))

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.68675621G>A
DNA change (hg38) -
Published as IGHMBP2(NM_002180.3):c.265G>A (p.V89M)
ISCN -
DB-ID IGHMBP2_000248
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) 1.0E-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
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)     

RNA change     

Protein     
IGHMBP2 NM_002180.2 ?/. - c.265G>A r.(?) p.(Val89Met)
MRPL21 NM_181514.1 ?/. - c.-4343C>T r.(?) p.(=)


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