Variant #0000350231 (NC_000001.10:g.46662456C>T, NM_001243766.1:c.301G>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.46662456C>T
DNA change (hg38) g.46196784C>T
Published as POMGNT1(NM_001243766.1):c.301G>A (p.V101I), POMGNT1(NM_001243766.2):c.301G>A (p.V101I)
ISCN -
DB-ID POMGNT1_000192 See all 4 reported entries
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) 0.00314 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +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.-6643C>T r.(?) p.(=)
POMGNT1 NM_001243766.1 -?/. - c.301G>A r.(?) p.(Val101Ile)
POMGNT1 NM_017739.3 -?/. - c.301G>A r.(?) p.(Val101Ile)


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