RGD:28881908 Rat Genome Database

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Variant: RGD:28881908 -  Homo sapiens

RGD ID: 28881908
RS ID: rs1564210000
ClinVar ID: CV900763
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FKTN  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 108,336,002
GRCh38 9 105,573,721
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001351502.2:c.-709G>A
LRG_434:g.20592G>A
NG_008754.1:g.20592G>A
NM_001079802.2:c.-114G>A
More... 		01/13/2018 5 prime utr variant uncertain significance CARDIOMYOPATHY, DILATED, WITH MILD OR NO PROXIMAL MUSCLE WEAKNESS; Cerebromuscular dystrophy, Fukuyama type; Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A4; FKTN-Related Dilated Cardiomyopathy; Fukuyama congenital muscular dystrophy; Fukuyama type muscular dystrophy; Muscular dystrophy, congenital progressive, with mental retardation; Muscular dystrophy, congenital, with central nervous system involvement; WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, FKTN-RELATED; Walker-Warburg syndrome, FKTN-related

Variant Details
Variant Transcripts
Gene Symbol:FKTN
Accession:NM_001351499
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422974
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422989
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422976
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422980
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_011518368
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422992
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_011518373
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422985
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422996
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:NM_001198963
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422987
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:NM_001351502
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422986
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422984
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422988
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:NM_001351500
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422998
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422970
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422995
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_011518391
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:NM_001351497
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422977
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047423001
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047423000
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422979
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422978
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422969
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047423002
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422968
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:NM_001079802
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:NM_001351496
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422975
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422971
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_011518369
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_017014462
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422967
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422973
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422999
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422991
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_047422994
Location:5UTRS;EXON

Gene Symbol:FKTN
Accession:XM_017014475
Location:5UTRS;INTRON

Gene Symbol:FKTN
Accession:XM_047422972
Location:5UTRS;INTRON

Gene Symbol:FKTN
Accession:NM_001351498
Location:5UTRS;INTRON

Gene Symbol:FKTN
Accession:XM_047422993
Location:5UTRS;INTRON

Gene Symbol:FKTN
Accession:NM_001351501
Location:5UTRS;INTRON

Gene Symbol:FKTN
Accession:XM_047422990
Location:5UTRS;INTRON

Gene Symbol:FKTN
Accession:XM_011518374
Location:5UTRS;INTRON

Gene Symbol:FKTN
Accession:XM_047422997
Location:5UTRS;INTRON

Gene Symbol:FKTN
Accession:NM_006731
Location:5UTRS;INTRON

Gene Symbol:FKTN
Accession:XM_006717014
Location:5UTRS;INTRON

Gene Symbol:FKTN
Accession:NR_147213
Location:EXON;NON-CODING

Gene Symbol:FKTN
Accession:XM_047422982
Location:INTRON

Gene Symbol:FKTN
Accession:XM_011518379
Location:INTRON

Gene Symbol:FKTN
Accession:XM_047422981
Location:INTRON

Gene Symbol:FKTN
Accession:XM_047422983
Location:INTRON

Gene Symbol:FKTN
Accession:NR_147214
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001167756 CLINVAR
  RCV001167757 CLINVAR
dbSNP (RS) rs1564210000 CLINVAR
MedGen C0410174 CLINVAR
  C1969024 CLINVAR
NCBI Gene FKTN CLINVAR
OMIM 253800 CLINVAR
  607440 CLINVAR
  611615 CLINVAR
SNOMED CT 111502003 CLINVAR