Variant #0000978186 (NC_000008.10:g.33361381G>C, NM_025115.3:c.1000C>G (TTI2))

Chromosome 8
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.33361381G>C
DNA change (hg38) -
Published as TTI2(NM_001102401.4):c.1000C>G (p.(Arg334Gly))
ISCN -
DB-ID MAK16_000009
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTI2 NM_025115.3 ?/. - c.1000C>G r.(?) p.(Arg334Gly)
MAK16 NM_032509.3 ?/. - c.*5234G>C r.(=) p.(=)


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