Variant #0000614431 (NC_000012.11:g.9085340_9085342dup, NM_001207024.1:c.*9087_*9089dup (M6PR))

Chromosome 12
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.9085340_9085342dup
DNA change (hg38) g.8932744_8932746dup
Published as PHC1(NM_004426.2):c.1271_1272insGCA (p.(Ala424_Gln425insGln)), PHC1(NM_004426.2):c.1287_1289dupGCA (p.Q439dup)
ISCN -
DB-ID M6PR_000003 See all 2 reported entries
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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
M6PR NM_001207024.1 -?/. - c.*9087_*9089dup r.(=) p.(=)
PHC1 NM_004426.2 -?/. - c.1287_1289dup r.(?) p.(Gln439dup)


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