Variant #0000544775 (NC_000011.9:g.62444430C>G, NM_024099.3:c.-5405G>C (C11orf48))

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.62444430C>G
DNA change (hg38) g.62676958C>G
Published as UBXN1(NM_015853.4):c.699G>C (p.R233=)
ISCN -
DB-ID C11orf48_000003
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) 0.00026 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-30 17:09:33 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C11orf83 NM_001085372.2 -?/. - c.*4844C>G r.(=) p.(=)
UBXN1 NM_015853.3 -?/. - c.699G>C r.(?) p.(Arg233=)
C11orf48 NM_024099.3 -?/. - c.-5405G>C r.(?) p.(=)


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