Variant #0000723534 (NC_000011.9:g.62383978C>T, NM_000327.3:c.*1667C>T (ROM1))

Chromosome 11
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.62383978C>T
DNA change (hg38) -
Published as B3GAT3(NM_001288723.1):c.909G>A (p.R303=)
ISCN -
DB-ID B3GAT3_000033
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ROM1 NM_000327.3 -?/. - c.*1667C>T r.(=) p.(=)
B3GAT3 NM_012200.3 -?/. - c.909G>A r.(?) p.(Arg303=)
EML3 NM_153265.2 -?/. - c.-4049G>A r.(?) p.(=)


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