Variant #0000527470 (NC_000006.11:g.152501416C>T, NM_182961.3:c.23315G>A (SYNE1))

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.152501416C>T
DNA change (hg38) g.152180281C>T
Published as SYNE1(NM_001347701.1):c.-80G>A (p.(=)), SYNE1(NM_182961.3):c.23315G>A (p.R7772Q), SYNE1(NM_182961.4):c.23315G>A (p.R7772Q)
ISCN -
DB-ID SYNE1_000921 See all 6 reported entries
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) 0.0035 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SYNE1 NM_182961.3 -?/. - c.23315G>A r.(?) p.(Arg7772Gln)


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