Variant #0000924443 (NC_000006.11:g.152651557G>A, NM_182961.3:c.14263C>T (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.152651557G>A
DNA change (hg38) -
Published as SYNE1(NM_033071.3):c.14050C>T (p.(Leu4684Phe)), SYNE1(NM_182961.3):c.14263C>T (p.L4755F), SYNE1(NM_182961.4):c.14263C>T (p.L4755F)
ISCN -
DB-ID SYNE1_000142 See all 17 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) 0.00093 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-04-16 21:50:28 +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     
SYNE1 NM_182961.3 -?/. - c.14263C>T r.(?) p.(Leu4755Phe)


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