Variant #0001032912 (NC_000002.11:g.208994322C>T, NM_006891.3:c.-5125G>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.208994322C>T
DNA change (hg38) -
Published as CRYGC(NM_020989.4):c.95G>A (p.(Arg32His))
ISCN -
DB-ID CRYGB_000037
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) 6.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.*13040G>A r.(=) p.(=)
CRYGD NM_006891.3 -?/. - c.-5125G>A r.(?) p.(=)
CRYGC NM_020989.3 -?/. - c.95G>A r.(?) p.(Arg32His)


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