Variant #0000306146 (NC_000001.10:g.46658910G>A, NC_000001.10(NM_001243766.1):c.1111-23C>T (POMGNT1))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46658910G>A
DNA change (hg38) g.46193238G>A
Published as POMGNT1(NM_017739.3):c.1111-23C>T
ISCN -
DB-ID POMGNT1_000033 See all 3 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) 0.06693 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 2020-03-23 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.-10189G>A r.(?) p.(=)
POMGNT1 NM_001243766.1 -/. - c.1111-23C>T r.(=) p.(=)
POMGNT1 NM_017739.3 -/. - c.1111-23C>T r.(=) p.(=)


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