Variant #0000807528 (NC_000016.9:g.68391047A>G, NM_019023.2:c.1999A>G (PRMT7))

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.68391047A>G
DNA change (hg38) -
Published as PRMT7(NM_001351143.1):c.1999A>G (p.T667A)
ISCN -
DB-ID SMPD3_000004
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) 0.00033 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     
SMPD3 NM_018667.3 -?/. - c.*4062T>C r.(=) p.(=)
PRMT7 NM_019023.2 -?/. - c.1999A>G r.(?) p.(Thr667Ala)


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