Variant #0000322424 (NC_000011.9:g.77612522T>C, INTS4(NM_033547.3):c.2173A>G)

Chromosome 11
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.77612522T>C
DNA change (hg38) g.77901476T>C
Published as INTS4(NM_033547.3):c.2173A>G (p.(Met725Val))
ISCN -
DB-ID INTS4_000002
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AAMDC NM_024684.2 ?/. - c.*29161T>C r.(=) p.(=)
INTS4 NM_033547.3 ?/. - c.2173A>G r.(?) p.(Met725Val)