Variant #0000681030 (NC_000017.10:g.74084902T>C, NM_001013839.2:c.1150A>G (EXOC7))

Chromosome 17
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.74084902T>C
DNA change (hg38) -
Published as EXOC7(NM_001145297.3):c.1303A>G (p.I435V)
ISCN -
DB-ID EXOC7_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) 2.0E-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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EXOC7 NM_001013839.2 -?/. - c.1150A>G r.(?) p.(Ile384Val)
ZACN NM_180990.3 -?/. - c.*6168T>C r.(=) p.(=)


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