Variant #0000688605 (NC_000002.11:g.208993027C>T, CRYGD(NM_006891.3):c.-3830G>A)

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.208993027C>T
DNA change (hg38) -
Published as CRYGC(NM_020989.3):c.425G>A (p.R142Q)
ISCN -
DB-ID CRYGB_000023
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYGB NM_005210.3 ?/. - c.*14335G>A r.(=) p.(=)
CRYGD NM_006891.3 ?/. - c.-3830G>A r.(?) p.(=)
CRYGC NM_020989.3 ?/. - c.425G>A r.(?) p.(Arg142Gln)