Variant #0000890012 (NC_000011.9:g.62382261G>A, NM_000327.3:c.1006G>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.62382261G>A
DNA change (hg38) -
Published as ROM1(NM_000327.3):c.1006G>A (p.E336K), ROM1(NM_000327.4):c.1006G>A (p.(Glu336Lys))
ISCN -
DB-ID ROM1_000011 See all 4 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) 8.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.1006G>A r.(?) p.(Glu336Lys)
B3GAT3 NM_012200.3 -?/. - c.*912C>T r.(=) p.(=)
EML3 NM_153265.2 -?/. - c.-2332C>T r.(?) p.(=)


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