Variant #0000528022 (NC_000006.11:g.170151766C>T, NC_000006.11(NM_018341.1):c.6+7C>T (C6orf70))

Chromosome 6
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.170151766C>T
DNA change (hg38) g.169751670C>T
Published as ERMARD(NM_018341.2):c.6+7C>T
ISCN -
DB-ID TCTE3_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) 0.16883 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C6orf70 NM_018341.1 -/. - c.6+7C>T r.(=) p.(=)
TCTE3 NM_174910.1 -/. - c.-212G>A r.(?) p.(=)


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