Variant #0000676449 (NC_000002.11:g.209007363C>T, NM_006891.3:c.-18166G>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.209007363C>T
DNA change (hg38) -
Published as CRYGB(NM_005210.3):c.527G>A (p.*176=)
ISCN -
DB-ID CRYGB_000022
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.527G>A r.(?) p.(Ter176=)
CRYGD NM_006891.3 -?/. - c.-18166G>A r.(?) p.(=)
CRYGC NM_020989.3 -?/. - c.-12847G>A r.(?) p.(=)


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