Variant #0000562072 (NC_000017.10:g.4462079_4462081del, NM_014520.3:c.-3460_-3458del (MYBBP1A))

Chromosome 17
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.4462079_4462081del
DNA change (hg38) g.4558784_4558786del
Published as GGT6(NM_001122890.2):c.713_715del (p.(Ala238del))
ISCN -
DB-ID GGT6_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     
SPNS2 NM_001124758.1 ?/. - c.*21336_*21338del r.(=) p.(=)
MYBBP1A NM_014520.3 ?/. - c.-3460_-3458del r.(?) p.(=)
GGT6 NM_153338.2 ?/. - c.617_619del r.(?) p.(Ala206del)


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