Variant #0000314531 (NC_000017.10:g.76109296C>T, NC_000017.10(NM_007267.6):c.2355-4G>A (TMC6))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.76109296C>T
DNA change (hg38) g.78113215C>T
Published as TMC6(NM_001127198.5):c.2355-4G>A
ISCN -
DB-ID TMC6_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) 0.01152 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMC6 NM_007267.6 -/. - c.2355-4G>A r.spl? p.?
TNRC6C NM_018996.3 -/. - c.*8370C>T r.(=) p.(=)
TMC8 NM_152468.4 -/. - c.-17945C>T r.(?) p.(=)


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