rs6741451 Rat Genome Database

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Variant: rs6741451 -  Homo sapiens

RGD ID: 150459563
RS ID: rs6741451
ClinVar ID: CV1264036
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127272329  MYT1L  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 1,842,787
GRCh38 2 1,839,015
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001329846.3:c.3074+134G>A
NM_001329847.2:c.3074+134G>A
NM_001329848.1:c.3074+134G>A
NM_001329849.3:c.3074+134G>A
More... 		04/01/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MYT1L
Accession:XM_011510322
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_017003612
Location:INTRON

Gene Symbol:MYT1L
Accession:NM_001329851
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_011510332
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_017003604
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_017003616
Location:INTRON

Gene Symbol:MYT1L
Accession:NM_001329849
Location:INTRON

Gene Symbol:MYT1L
Accession:NM_001329847
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_011510326
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_011510328
Location:INTRON

Gene Symbol:MYT1L
Accession:NM_001329844
Location:INTRON

Gene Symbol:MYT1L
Accession:NM_001303052
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_017003607
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_011510319
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_017003615
Location:INTRON

Gene Symbol:MYT1L
Accession:NM_001329846
Location:INTRON

Gene Symbol:MYT1L
Accession:NM_015025
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_011510318
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_011510323
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_011510331
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_017003605
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_011510320
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_011510321
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_017003621
Location:INTRON

Gene Symbol:MYT1L
Accession:NM_001329848
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_011510324
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_017003622
Location:INTRON

Gene Symbol:MYT1L
Accession:NM_001329852
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_011510327
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_017003608
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_017003606
Location:INTRON

Gene Symbol:MYT1L
Accession:NM_001329845
Location:INTRON

Gene Symbol:MYT1L
Accession:XM_017003620
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001681951 CLINVAR
dbSNP (RS) rs6741451 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MYT1L CLINVAR
OMIM 613084 CLINVAR