Variant #0000307196 (NC_000011.9:g.62380931C>A, NM_000327.3:c.178C>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.62380931C>A
DNA change (hg38) g.62613459C>A
Published as ROM1(NM_000327.3):c.178C>A (p.P60T)
ISCN -
DB-ID ROM1_000004 See all 9 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) 0.00021 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +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.178C>A r.(?) p.(Pro60Thr)
B3GAT3 NM_012200.3 -?/. - c.*2242G>T r.(=) p.(=)
EML3 NM_153265.2 -?/. - c.-1002G>T r.(?) p.(=)


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