Variant #0000971624 (NC_000002.11:g.224824269_224824276delinsTA, NM_022915.3:c.198_205delinsTA (MRPL44))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.224824269_224824276delinsTA
DNA change (hg38) -
Published as -
ISCN -
DB-ID MRPL44_000006
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-03-09 11:31:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRPL44 NM_022915.3 +?/. - c.198_205delinsTA r.(?) p.(Trp66_His69delinsCysAsn)


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