Variant #0000691108 (NC_000011.9:g.62557476C>G, NM_199337.2:c.617C>G (TMEM179B))

Chromosome 11
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.62557476C>G
DNA change (hg38) -
Published as TMEM179B(NM_199337.3):c.617C>G (p.S206C)
ISCN -
DB-ID NXF1_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) 0.00011 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM223 NM_001080501.2 ?/. - c.*619G>C r.(=) p.(=)
NXF1 NM_006362.4 ?/. - c.*2472G>C r.(=) p.(=)
TAF6L NM_006473.3 ?/. - c.*2708C>G r.(=) p.(=)
TMEM179B NM_199337.2 ?/. - c.617C>G r.(?) p.(Ser206Cys)


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