Variant #0000974876 (NC_000002.11:g.208989179C>G, NC_000002.11(NM_006891.3):c.9+10G>C (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.208989179C>G
DNA change (hg38) -
Published as CRYGD(NM_006891.4):c.9+10G>C
ISCN -
DB-ID CRYGB_000031
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) 0.0001 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 2024-04-19 20:20:39 +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.*18183G>C r.(=) p.(=)
CRYGD NM_006891.3 -?/. - c.9+10G>C r.(=) p.(=)
CRYGC NM_020989.3 -?/. - c.*3748G>C r.(=) p.(=)


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