Variant #0000274466 (NC_000002.11:g.208992979C>T, NM_006891.3:c.-3782G>A (CRYGD))

Chromosome 2
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.208992979C>T
DNA change (hg38) g.208128255C>T
Published as CRYGC(NM_020989.3):c.473G>A (p.G158E)
ISCN -
DB-ID CRYGC_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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYGB NM_005210.3 ?/. - c.*14383G>A r.(=) p.(=)
CRYGD NM_006891.3 ?/. - c.-3782G>A r.(?) p.(=)
CRYGC NM_020989.3 ?/. - c.473G>A r.(?) p.(Gly158Glu)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.