Variant #0000327154 (NC_000002.11:g.86832291G>T, NM_022780.3:c.-115500G>T (RMND5A))

Chromosome 2
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.86832291G>T
DNA change (hg38) g.86605168G>T
Published as RNF103(NM_001198951.1):c.721C>A (p.(Gln241Lys))
ISCN -
DB-ID RNF103_000002
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 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 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     
RNF103-CHMP3 NM_001198954.1 ?/. - c.132+15162C>A r.(=) p.(=)
RNF103 NM_005667.3 ?/. - c.733C>A r.(?) p.(Gln245Lys)
CHMP3 NM_016079.3 ?/. - c.-41820C>A r.(?) p.(=)
RMND5A NM_022780.3 ?/. - c.-115500G>T r.(?) p.(=)


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