Variant #0000306150 (NC_000001.10:g.46657986C>T, NM_001243766.1:c.1407G>A (POMGNT1))

Chromosome 1
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.46657986C>T
DNA change (hg38) g.46192314C>T
Published as POMGNT1(NM_017739.3):c.1407G>A (p.P469=)
ISCN -
DB-ID POMGNT1_000167
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) 3.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LURAP1 NM_001013615.2 -?/. - c.-11113C>T r.(?) p.(=)
POMGNT1 NM_001243766.1 -?/. - c.1407G>A r.(?) p.(Pro469=)
POMGNT1 NM_017739.3 -?/. - c.1407G>A r.(?) p.(Pro469=)


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