Variant #0000677642 (NC_000006.11:g.139266669G>A, NM_001077706.2:c.*42905G>A (ECT2L))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.139266669G>A
DNA change (hg38) -
Published as REPS1(NM_001286611.1):c.443C>T (p.T148M)
ISCN -
DB-ID ECT2L_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) 0.00049 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ECT2L NM_001077706.2 -?/. - c.*42905G>A r.(=) p.(=)
REPS1 NM_001128617.1 -?/. - c.443C>T r.(?) p.(Thr148Met)


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