Variant #0000544757 (NC_000011.9:g.62381934A>T, NM_000327.3:c.795A>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.62381934A>T
DNA change (hg38) g.62614462A>T
Published as ROM1(NM_000327.3):c.795A>T (p.A265=)
ISCN -
DB-ID B3GAT3_000013
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-30 17:02:36 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ROM1 NM_000327.3 -?/. - c.795A>T r.(?) p.(Ala265=)
B3GAT3 NM_012200.3 -?/. - c.*1239T>A r.(=) p.(=)
EML3 NM_153265.2 -?/. - c.-2005T>A r.(?) p.(=)


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