Variant #0000545526 (NC_000011.9:g.68671290_68671291insTTCCCGCGCCTC, NM_002180.2:c.-131_-130insTTCCCGCGCCTC (IGHMBP2))

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.68671290_68671291insTTCCCGCGCCTC
DNA change (hg38) g.68903822_68903823insTTCCCGCGCCTC
Published as MRPL21(NM_181515.2):c.-276_-275insGCGGGAAGAGGC
ISCN -
DB-ID IGHMBP2_000173
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
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGHMBP2 NM_002180.2 -/. - c.-131_-130insTTCCCGCGCCTC r.(?) p.(=)
MRPL21 NM_181514.1 -/. - c.-8_-7insGCGGGAAGAGGC r.(?) p.(=)


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