Variant #0000529996 (NC_000006.11:g.90338915_90338934del, NM_020466.4:c.*8060_*8079del (LYRM2))

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.90338915_90338934del
DNA change (hg38) g.89629196_89629215del
Published as ANKRD6(NM_001242811.1):c.1570_1589delTGCAGAGCTAAATCCACACC (p.C524Ifs*4)
ISCN -
DB-ID ANKRD6_000002
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-19 19:28:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD6 NM_001242809.1 ?/. - c.1570_1589del r.(?) p.(Cys524IlefsTer4)
LYRM2 NM_020466.4 ?/. - c.*8060_*8079del r.(=) p.(=)


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