Variant #0000297709 (NC_000011.9:g.62381106G>C, NM_000327.3:c.353= (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.62381106G>C
DNA change (hg38) g.62613634G>C
Published as ROM1(NM_000327.4):c.353G>C (p.G118A)
ISCN -
DB-ID ROM1_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) 0.98509 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.353= r.(=) p.(Ala118=)
B3GAT3 NM_012200.3 -/. - c.*2067C>G r.(=) p.(=)
EML3 NM_153265.2 -/. - c.-1177C>G r.(?) p.(=)


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