Variant #0000571592 (NC_000022.10:g.25024045C>T, NC_000022.10(NM_013430.2):c.1337-3C>T (GGT1))

Chromosome 22
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.25024045C>T
DNA change (hg38) g.24628078C>T
Published as GGT1(NM_001288833.2):c.1337-3C>T
ISCN -
DB-ID FAM211B_000004
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) 0.00054 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-17 11:49:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GGT1 NM_013430.2 ?/. - c.1337-3C>T r.spl? p.?
FAM211B NM_207644.2 ?/. - c.-35039G>A r.(?) p.(=)


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