Variant #0000520298 (NC_000003.11:g.51430056T>C, NM_006010.4:c.*3536T>C (MANF))

Chromosome 3
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.51430056T>C
DNA change (hg38) g.51392625T>C
Published as RBM15B(NM_013286.4):c.1226T>C (p.(Ile409Thr))
ISCN -
DB-ID MANF_000001
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
MANF NM_006010.4 ?/. - c.*3536T>C r.(=) p.(=)
RBM15B NM_013286.4 ?/. - c.1226T>C r.(?) p.(Ile409Thr)
VPRBP NM_014703.2 ?/. - c.*4534A>G r.(=) p.(=)


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