Variant #0000620656 (NC_000001.10:g.46659986C>T, NM_001243766.1:c.839G>A (POMGNT1))

Chromosome 1
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.46659986C>T
DNA change (hg38) g.46194314C>T
Published as POMGNT1(NM_001243766.1):c.839G>A (p.S280N)
ISCN -
DB-ID POMGNT1_000220 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) 0.00024 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 2019-12-06 12:43:26 +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     
LURAP1 NM_001013615.2 ?/. - c.-9113C>T r.(?) p.(=)
POMGNT1 NM_001243766.1 ?/. - c.839G>A r.(?) p.(Ser280Asn)
POMGNT1 NM_017739.3 ?/. - c.839G>A r.(?) p.(Ser280Asn)


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