Variant #0000909028 (NC_000016.9:g.2806333A>T, NC_000016.9(NM_016333.3):c.-31-2A>T (SRRM2))

Chromosome 16
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.2806333A>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SRRM2_000031
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-12-21 15:28:01 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRRM2 NM_016333.3 ?/. - c.-31-2A>T r.(?) p.(?)


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