Variant #0001056194 (NC_000017.10:g.74084639G>A, NM_001013839.2:c.1205C>T (EXOC7))

Chromosome 17
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.74084639G>A
DNA change (hg38) -
Published as EXOC7(NM_001013839.4):c.1205C>T (p.(Thr402Met))
ISCN -
DB-ID ZACN_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) 0.00018 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 2025-11-01 13:22:20 +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     
EXOC7 NM_001013839.2 ?/. - c.1205C>T r.(?) p.(Thr402Met)
ZACN NM_180990.3 ?/. - c.*5905G>A r.(=) p.(=)


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