Variant #0001046947 (NC_000016.9:g.2814425C>T, NM_016333.3:c.3896C>T (SRRM2))

Chromosome 16
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.2814425C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SRRM2_000112
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs202093728
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-07-14 11:06:01 +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     
SRRM2 NM_016333.3 -?/. - c.3896C>T r.(?) p.(Pro1299Leu)


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