Variant #0001033953 (NC_000003.11:g.39178505G>A, NM_145755.2:c.3232G>A (TTC21A))

Chromosome 3
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.39178505G>A
DNA change (hg38) -
Published as TTC21A(NM_001366900.1):c.3211G>A (p.(Glu1071Lys))
ISCN -
DB-ID CSRNP1_000005
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) 0.00043 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
CSRNP1 NM_033027.3 ?/. - c.*6041C>T r.(=) p.(=)
TTC21A NM_145755.2 ?/. - c.3232G>A r.(?) p.(Glu1078Lys)


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