Variant #0000306158 (NC_000001.10:g.46659524T>C, NC_000001.10(NM_001243766.1):c.950+3A>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.46659524T>C
DNA change (hg38) g.46193852T>C
Published as POMGNT1(NM_017739.3):c.950+3A>G
ISCN -
DB-ID POMGNT1_000174
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) Retrieve
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 2020-06-04 14:00:28 +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.-9575T>C r.(?) p.(=)
POMGNT1 NM_001243766.1 -?/. - c.950+3A>G r.spl? p.?
POMGNT1 NM_017739.3 -?/. - c.950+3A>G r.spl? p.?


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