Variant #0000552844 (NC_000014.8:g.65419244A>G, NC_000014.8(NM_001202558.1):c.6+28400A>G (CHURC1-FNTB))

Chromosome 14
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.65419244A>G
DNA change (hg38) g.64952526A>G
Published as RAB15(NM_001330182.1):c.32T>C (p.V11A)
ISCN -
DB-ID CHURC1_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) Retrieve
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHURC1-FNTB NM_001202558.1 ?/. - c.6+28400A>G r.(=) p.(=)
FNTB NM_002028.3 ?/. - c.-34428A>G r.(?) p.(=)
GPX2 NM_002083.3 ?/. - c.-9800T>C r.(?) p.(=)
CHURC1 NM_145165.3 ?/. - c.*20296A>G r.(=) p.(=)
RAB15 NM_198686.2 ?/. - c.170T>C r.(?) p.(Val57Ala)


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