Variant #0000605813 (NC_000001.10:g.46659302G>C, NM_001243766.1:c.960C>G (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.46659302G>C
DNA change (hg38) g.46193630G>C
Published as POMGNT1(NM_001243766.1):c.960C>G (p.R320=), POMGNT1(NM_001243766.2):c.960C>G (p.R320=)
ISCN -
DB-ID LURAP1_000007 See all 2 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) 0.00012 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.-9797G>C r.(?) p.(=)
POMGNT1 NM_001243766.1 -?/. - c.960C>G r.(?) p.(Arg320=)
POMGNT1 NM_017739.3 -?/. - c.960C>G r.(?) p.(Arg320=)


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