Variant #0000322268 (NC_000011.9:g.62414052A>C, NM_198335.3:c.20T>G (GANAB))

Chromosome 11
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.62414052A>C
DNA change (hg38) g.62646580A>C
Published as GANAB(NM_001278192.1):c.20T>G (p.(Val7Gly))
ISCN -
DB-ID GANAB_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) 0.00014 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
INTS5 NM_030628.1 ?/. - c.*440T>G r.(=) p.(=)
GANAB NM_198335.3 ?/. - c.20T>G r.(?) p.(Val7Gly)


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