Variant #0000000935 (NC_000006.12:g.152505243C>T, NM_182961.3:c.736G>A (SYNE1))

Individual ID 00000188
Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.152505243C>T
Published as A246T
Reference Shafina-Nadiawati Abdul et al. (2017)dbSNP
DB-ID SYNE1_000008
dbSNP ID rs1251834592
Frequency 1/9
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2020-11-25 14:54:36 +08:00 (CST)
Date last edited 2021-08-23 15:25:32 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

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DNA change (cDNA)     

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GVS function     

Clinical classification     
SYNE1 NM_182961.3 ?/. 9 c.736G>A - r.(?) p.(Ala246Thr) - ClinVar



Screenings


AscendingScreening ID     

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Genes screened     

Variants found     

Owner     
0000000203 DNA PCR;SEQ;Western SYNE1 9 Nuur Athirah Binti Mohd Daud