Variant #0000528233 (NC_000006.11:g.30997605_30997616del, NM_001198815.1:c.4397_4408del (MUC22))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.30997605_30997616del
DNA change (hg38) g.31029828_31029839del
Published as MUC22(NM_001198815.1):c.4397_4408del (p.(Asn1466_Cys1469del))
ISCN -
DB-ID MUC22_000010
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MUC22 NM_001198815.1 -?/. - c.4397_4408del r.(?) p.(Asn1466_Cys1469del)


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