Variant #0000570514 (NC_000021.8:g.34012088G>A, NM_203446.2:c.3707C>T (SYNJ1))

Chromosome 21
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.34012088G>A
DNA change (hg38) g.32639778G>A
Published as SYNJ1(NM_003895.3):c.3707C>T (p.T1236M), SYNJ1(NM_203446.2):c.3707C>T (p.T1236M)
ISCN -
DB-ID SYNJ1_000037 See all 2 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) 0.00148 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SYNJ1 NM_203446.2 -?/. - c.3707C>T r.(?) p.(Thr1236Met)


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