Variant #0000858248 (NC_000002.11:g.209007492A>C, NM_006891.3:c.-18295T>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.209007492A>C
DNA change (hg38) -
Published as CRYGB(NM_005210.3):c.398T>G (p.I133S)
ISCN -
DB-ID CRYGB_000027
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYGB NM_005210.3 ?/. - c.398T>G r.(?) p.(Ile133Ser)
CRYGD NM_006891.3 ?/. - c.-18295T>G r.(?) p.(=)
CRYGC NM_020989.3 ?/. - c.-12976T>G r.(?) p.(=)


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