Variant #0000320965 (NC_000001.10:g.149903313C>T, NM_005850.4:c.-3662G>A (SF3B4))

Chromosome 1
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.149903313C>T
DNA change (hg38) g.149931421C>T
Published as MTMR11(NM_001145862.1):c.1129G>A (p.(Gly377Ser))
ISCN -
DB-ID MTMR11_000002
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) 3.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTMR11 NM_001145862.1 -?/. - c.1129G>A r.(?) p.(Gly377Ser)
SF3B4 NM_005850.4 -?/. - c.-3662G>A r.(?) p.(=)
MTMR11 NM_181873.3 -?/. - c.913G>A r.(?) p.(Gly305Ser)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.