Variant #0000256144 (NC_000002.11:g.55195386A>T, NM_001039753.2:c.5720A>T (EML6))

Chromosome 2
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.55195386A>T
DNA change (hg38) g.54968250A>T
Published as EML6(NM_001039753.2):c.5720A>T (p.K1907M)
ISCN -
DB-ID EML6_000004
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EML6 NM_001039753.2 ?/. - c.5720A>T r.(?) p.(Lys1907Met)
RTN4 NM_007008.2 ?/. - c.*4906T>A r.(=) p.(=)


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