Variant #0000979695 (NC_000011.9:g.62382181A>C, NM_000327.3:c.926A>C (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.62382181A>C
DNA change (hg38) -
Published as ROM1(NM_000327.4):c.926A>C (p.(Tyr309Ser))
ISCN -
DB-ID B3GAT3_000043
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) 5.0E-5 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ROM1 NM_000327.3 ?/. - c.926A>C r.(?) p.(Tyr309Ser)
B3GAT3 NM_012200.3 ?/. - c.*992T>G r.(=) p.(=)
EML3 NM_153265.2 ?/. - c.-2252T>G r.(?) p.(=)


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