Variant #0000923800 (NC_000003.11:g.100467232C>G, NM_001007565.2:c.1060C>G (TFG))

Chromosome 3
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.100467232C>G
DNA change (hg38) -
Published as TFG(NM_001195479.1):c.1048C>G (p.P350A), TFG(NM_006070.6):c.1060C>G (p.P354A)
ISCN -
DB-ID ABI3BP_000011 See all 4 reported entries
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) 0.0012 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +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     
TFG NM_001007565.2 -?/. - c.1060C>G r.(?) p.(Pro354Ala)
ABI3BP NM_015429.3 -?/. - c.*2107G>C r.(=) p.(=)


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