Variant #0000615868 (NC_000016.9:g.2260601_2260603dup, NM_022372.4:c.*1723_*1725dup (MLST8))

Chromosome 16
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.2260601_2260603dup
DNA change (hg38) g.2210600_2210602dup
Published as BRICD5(NM_182563.3):c.117_118insCTG (p.(Leu39dup))
ISCN -
DB-ID MLST8_000005
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 2019-12-04 15:24:38 +01:00 (CET)
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     
PGP NM_001042371.2 -?/. - c.*3141_*3143dup r.(=) p.(=)
MLST8 NM_022372.4 -?/. - c.*1723_*1725dup r.(=) p.(=)
BRICD5 NM_182563.3 -?/. - c.115_117dup r.(?) p.(Leu39dup)


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