Variant #0000992398 (NC_000002.11:g.208993118T>A, NM_006891.3:c.-3921A>T (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.208993118T>A
DNA change (hg38) -
Published as CRYGC(NM_020989.3):c.334A>T (p.(Ile112Phe))
ISCN -
DB-ID CRYGB_000033
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +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.*14244A>T r.(=) p.(=)
CRYGD NM_006891.3 -?/. - c.-3921A>T r.(?) p.(=)
CRYGC NM_020989.3 -?/. - c.334A>T r.(?) p.(Ile112Phe)


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