Variant #0000654978 (NC_000003.11:g.48488452C>T, NM_016381.4:c.-19438C>T (TREX1))

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.48488452C>T
DNA change (hg38) g.48447048C>T
Published as ATRIP(NM_130384.3):c.203C>T (p.S68L)
ISCN -
DB-ID ATRIP_000045
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) 9.0E-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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMA7 NM_015933.3 ?/. - c.*3162C>T r.(=) p.(=)
TREX1 NM_016381.4 ?/. - c.-19438C>T r.(?) p.(=)
TREX1 NM_033629.3 ?/. - c.-19283C>T r.(?) p.(=)
ATRIP NM_130384.2 ?/. - c.203C>T r.(?) p.(Ser68Leu)


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