Variant #0000294886 (NC_000011.9:g.62381825G>A, NM_000327.3:c.686G>A (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.62381825G>A
DNA change (hg38) g.62614353G>A
Published as ROM1(NM_000327.3):c.686G>A (p.(Arg229His)), ROM1(NM_000327.4):c.686G>A (p.R229H)
ISCN -
DB-ID ROM1_000010 See all 12 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) 0.00345 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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.686G>A r.(?) p.(Arg229His)
B3GAT3 NM_012200.3 -?/. - c.*1348C>T r.(=) p.(=)
EML3 NM_153265.2 -?/. - c.-1896C>T r.(?) p.(=)


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