Variant #0000923565 (NC_000002.11:g.208994280T>C, NM_006891.3:c.-5083A>G (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.208994280T>C
DNA change (hg38) -
Published as CRYGC(NM_020989.4):c.137A>G (p.Y46C)
ISCN -
DB-ID CRYGB_000029
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) 3.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYGB NM_005210.3 ?/. - c.*13082A>G r.(=) p.(=)
CRYGD NM_006891.3 ?/. - c.-5083A>G r.(?) p.(=)
CRYGC NM_020989.3 ?/. - c.137A>G r.(?) p.(Tyr46Cys)


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