Variant #0000350162 (NC_000002.11:g.208988900T>C, CRYGD(NM_006891.3):c.188A>G)

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.208988900T>C
DNA change (hg38) g.208124176T>C
Published as -
ISCN -
DB-ID CRYGD_000034
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 5.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYGB NM_005210.3 -?/. - c.*18462A>G r.(=) p.(=)
CRYGD NM_006891.3 -?/. - c.188A>G r.(?) p.(Tyr63Cys)
CRYGC NM_020989.3 -?/. - c.*4027A>G r.(=) p.(=)