Variant #0000614432 (NC_000012.11:g.9085564C>G, NM_001207024.1:c.*8850G>C (M6PR))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.9085564C>G
DNA change (hg38) g.8932968C>G
Published as PHC1(NM_004426.2):c.1511C>G (p.(Pro504Arg))
ISCN -
DB-ID M6PR_000008
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     
M6PR NM_001207024.1 ?/. - c.*8850G>C r.(=) p.(=)
PHC1 NM_004426.2 ?/. - c.1511C>G r.(?) p.(Pro504Arg)


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