Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar01445249

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01445249EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01445249
Other_nameT08A11.1d.1:c.1335+32T>A
T08A11.1h.1:c.1335+32T>A
T08A11.1b.1:c.1335+32T>A
T08A11.1f.1:c.1335+32T>A
T08A11.1c.1:c.1335+32T>A
T08A11.1e.1:c.1335+32T>A
T08A11.1g.1:c.1335+32T>A
T08A11.1a.1:c.1335+32T>A
HGVSgCHROMOSOME_III:g.4259540A>T
Sequence_detailsSMapS_parentSequenceT08A11
Flanking_sequencesTTGCAAAACAATTTTTTTTCGTTTTTTTTTAATTTTCAAAAAAAAAGTCCAATCGTCTCA
Mapping_targetT08A11
Type_of_mutationSubstitutionat
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00031279From_analysisWGS_Andersen
WBStrain00031284From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisWGS_Andersen
DB_infoDatabasedbSNP_rsrs193332388
dbSNP_ssss295508307
StatusLive
AffectsGeneWBGene00011604
TranscriptT08A11.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1e.1:c.1335+32T>A
Intron_number6/17
T08A11.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1g.1:c.1335+32T>A
Intron_number7/18
T08A11.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1h.1:c.1335+32T>A
Intron_number7/18
T08A11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1d.1:c.1335+32T>A
Intron_number7/18
T08A11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1f.1:c.1335+32T>A
Intron_number6/17
T08A11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1c.1:c.1335+32T>A
Intron_number6/17
T08A11.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1b.1:c.1335+32T>A
Intron_number7/18
T08A11.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1a.1:c.1335+32T>A
Intron_number7/18
ReferenceWBPaper00040707
MethodWGS_Andersen