Variant #0000690069 (NC_000007.13:g.75611562T>C, NM_000941.2:c.752T>C (POR))

Chromosome 7
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.75611562T>C
DNA change (hg38) -
Published as POR(NM_000941.2):c.752T>C (p.(Val251Ala))
ISCN -
DB-ID POR_000108
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
POR NM_000941.2 -?/. - c.752T>C - r.(?) p.(Val251Ala)
TMEM120A NM_031925.2 -?/. - c.*4928A>G - r.(=) p.(=)


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