Variant #0000528023 (NC_000006.11:g.170154127A>G, NM_018341.1:c.174A>G (C6orf70))

Chromosome 6
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.170154127A>G
DNA change (hg38) g.169754031A>G
Published as ERMARD(NM_018341.2):c.174A>G (p.S58=)
ISCN -
DB-ID TCTE3_000003
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 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.174A>G r.(?) p.(Ser58=)
TCTE3 NM_174910.1 ?/. - c.-2573T>C r.(?) p.(=)


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