Variant #0000723533 (NC_000011.9:g.62383715G>C, NM_000327.3:c.*1404G>C (ROM1))

Chromosome 11
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.62383715G>C
DNA change (hg38) -
Published as B3GAT3(NM_001288723.2):c.910-3C>G
ISCN -
DB-ID B3GAT3_000032
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ROM1 NM_000327.3 -/. - c.*1404G>C r.(=) p.(=)
B3GAT3 NM_012200.3 -/. - c.909+263C>G r.(=) p.(=)
EML3 NM_153265.2 -/. - c.-3786C>G r.(?) p.(=)


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