Variant #0000514027 (NC_000002.11:g.209010498C>T, NM_006891.3:c.-21301G>A (CRYGD))

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.209010498C>T
DNA change (hg38) g.208145774C>T
Published as -
ISCN -
DB-ID CRYGB_000018
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) 7.0E-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
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYGB NM_005210.3 -?/. - c.252G>A r.(?) p.(Pro84=)
CRYGD NM_006891.3 -?/. - c.-21301G>A r.(?) p.(=)
CRYGC NM_020989.3 -?/. - c.-15982G>A r.(?) p.(=)


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