Variant #0000805977 (NC_000012.11:g.9086964G>T, NM_001207024.1:c.*7450C>A (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.9086964G>T
DNA change (hg38) -
Published as PHC1(NM_004426.2):c.2143G>T (p.V715L)
ISCN -
DB-ID M6PR_000011
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) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.*7450C>A r.(=) p.(=)
PHC1 NM_004426.2 -?/. - c.2143G>T r.(?) p.(Val715Leu)


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