Variant #0000559367 (NC_000016.9:g.841874G>A, NM_022092.2:c.1128G>A (CHTF18))

Chromosome 16
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.841874G>A
DNA change (hg38) g.791874G>A
Published as CHTF18(NM_022092.3):c.1128G>A (p.P376=)
ISCN -
DB-ID CHTF18_000015
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) 0.00015 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 2020-07-07 12:20:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNG13 NM_016541.2 ?/. - c.*6845C>T r.(=) p.(=)
CHTF18 NM_022092.2 ?/. - c.1128G>A r.(?) p.(Pro376=)
RPUSD1 NM_058192.2 ?/. - c.-3626C>T r.(?) p.(=)


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