Variant #0000613486 (NC_000011.9:g.62383252C>G, NM_000327.3:c.*941C>G (ROM1))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.62383252C>G
DNA change (hg38) g.62615780C>G
Published as B3GAT3(NM_012200.3):c.929G>C (p.(Arg310Pro))
ISCN -
DB-ID B3GAT3_000025
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +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     
ROM1 NM_000327.3 ?/. - c.*941C>G r.(=) p.(=)
B3GAT3 NM_012200.3 ?/. - c.929G>C r.(?) p.(Arg310Pro)
EML3 NM_153265.2 ?/. - c.-3323G>C r.(?) p.(=)


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