Variant #0000519789 (NC_000003.11:g.39185201G>A, NM_145755.2:c.*4922G>A (TTC21A))

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.39185201G>A
DNA change (hg38) g.39143710G>A
Published as CSRNP1(NM_001320559.1):c.1175C>T (p.P392L)
ISCN -
DB-ID CSRNP1_000001
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) 4.0E-5 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSRNP1 NM_033027.3 -?/. - c.1115C>T r.(?) p.(Pro372Leu)
TTC21A NM_145755.2 -?/. - c.*4922G>A r.(=) p.(=)


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