Variant #0000260316 (NC_000011.9:g.62384066G>T, NM_000327.3:c.*1755G>T (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.62384066G>T
DNA change (hg38) g.62616594G>T
Published as B3GAT3(NM_012200.3):c.821C>A (p.(Thr274Asn)), B3GAT3(NM_012200.4):c.821C>A (p.T274N)
ISCN -
DB-ID B3GAT3_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) 0.00127 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +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     
ROM1 NM_000327.3 -/. - c.*1755G>T r.(=) p.(=)
B3GAT3 NM_012200.3 -/. - c.821C>A r.(?) p.(Thr274Asn)
EML3 NM_153265.2 -/. - c.-4137C>A r.(?) p.(=)


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