http://identifiers.org/hco/22/GRCh38#34756720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75224145-A-C

http://identifiers.org/hco/22/GRCh38#34756730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75224155-C-A

34756763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: non coding transcript exon variant
orthologous variants: 75224191-T-A

34757026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: non coding transcript exon variant
orthologous variants: 75224450-G-A

34757026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: non coding transcript exon variant
orthologous variants: 75224450-G-T

34757103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: non coding transcript exon variant
orthologous variants: 75224506-C-T

34757281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: non coding transcript exon variant
orthologous variants: 75224878-C-G

34757281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: non coding transcript exon variant
orthologous variants: 75224878-C-T

34757390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: non coding transcript exon variant
orthologous variants: 75224970-G-T

34757406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: non coding transcript exon variant
orthologous variants: 75224986-T-C

34757651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: non coding transcript exon variant
orthologous variants: 75225210-T-C

34759655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75226375-G-A

34759734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75226452-G-A

34759824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75226546-G-A

http://identifiers.org/hco/22/GRCh38#34760102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75226784-C-A

34760300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75227075-C-T

34760328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75227103-G-T

34760453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75227244-T-G

34760575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75227367-A-G

34760995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75227803-C-G

34761053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75227858-C-T

34761139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75227943-A-T

34761418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75228210-G-A

34761917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75228686-T-C

34761947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75228716-G-C

34761975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75228750-A-G

34762113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75228882-G-A

34762501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75229097-T-C

34762523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75229119-G-A

34762523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75229119-G-T

http://identifiers.org/hco/22/GRCh38#34762589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75229188-C-A

34762710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75229300-C-T

34762831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75229472-T-C

34762928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75229998-G-A

34763194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75230183-G-T

34763240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75230217-C-T

34763335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75230259-C-T

34764581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75231580-T-C

34764616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75231615-G-A

34764636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75231632-C-T

34764737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75231741-T-A

34764737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75231741-T-C

34765030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75232370-G-A

34765208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75232525-G-A

34765208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75232525-G-T

34765776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233041-G-T

34765882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233126-T-G

http://identifiers.org/hco/22/GRCh38#34766329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75233497-C-A

34766400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233569-G-A

34766400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233569-G-T

34766405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233593-C-G

34766482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233667-C-G

34766586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233754-G-A

34766705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233874-C-G

34766705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233874-C-T

34766770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233934-G-C

34766780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233944-A-T

34766791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233956-G-A

34766802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75233974-A-G

34766925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75234129-T-C

http://identifiers.org/hco/22/GRCh38#34767253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75234696-A-C

34767262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75234705-T-C

34767263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75234706-G-A

34767268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75234711-A-G

34767282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75234725-G-A

34767282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75234725-G-C

34767350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75234784-G-A

34767554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75234983-G-A

34767767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75235189-C-G

34767899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75235318-C-T

34768023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75235433-G-A

34768657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75247883-T-A

34768668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75247894-G-A

34768669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75247895-A-T

34769044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248135-G-A

http://identifiers.org/hco/22/GRCh38#34769256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75248300-C-A

34769728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248763-T-C

34769746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75248779-C-T

34770086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249124-A-G

34770101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249136-A-G

34770130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249165-T-C

34770139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249174-A-G

34770321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249363-G-C

34770445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249494-G-A

34770534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249574-G-A

34770561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249601-A-T

34770969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75249986-A-G

34771029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75250035-G-A

34771453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75250470-G-A

34771631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75250645-G-A

34771631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75250645-G-T

34771822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75250788-C-T

34772779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75255836-G-T

34772815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75255868-G-A

34772917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75255957-G-T

34772957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75255988-T-C

http://identifiers.org/hco/22/GRCh38#34773182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75256288-A-C

34773255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75256353-G-A

34773704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75256737-T-C

34774275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75257006-G-A

34774593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75257256-C-T

34774662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75257320-G-C

34774997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75257616-C-T

34775334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75257919-A-G

34775454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75258151-C-T

34775516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75258213-G-A

34775622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75258306-C-T

34775756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75258431-T-C

http://identifiers.org/hco/22/GRCh38#34775891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75258552-C-A

34775983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75258594-T-C

http://identifiers.org/hco/22/GRCh38#34776143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75258622-C-A

34776426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75258724-G-A

34776455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75258758-G-C

34776455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75258758-G-T

34776531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75258829-G-A

34776745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75259010-G-A

34776820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75259082-T-A

34776820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75259082-T-C

34776908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75259168-T-C

34776971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75259229-T-C

34783973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75280334-G-C

34783986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75280345-A-T

34787804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75280773-T-A

34787807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75280775-A-T

http://identifiers.org/hco/22/GRCh38#34787813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75280781-A-C

34787813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75280781-A-G

34787813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75280781-A-T

34787916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75280880-G-T

34787936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75280900-C-T

http://identifiers.org/hco/22/GRCh38#34787946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75280960-C-A

34787946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75280960-C-T

34787996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75281008-T-C

34788345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75281316-T-A

34788345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75281316-T-C

34794996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75281530-A-G

34795061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75281595-G-A

34795061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75281595-G-C

34795250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75281781-C-T

34795335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75281859-C-T

34795530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75281966-G-A

34795530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75281966-G-C

34795530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75281966-G-T

34795587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282020-A-G

34795856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282285-T-A

34795857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282286-G-A

34796231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282509-G-A

34799073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75282987-T-G

34799134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75283042-T-C

http://identifiers.org/hco/22/GRCh38#34799348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75283095-C-A

34799431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75283157-G-A

34799688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75284063-G-A

34799731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75284110-T-G

34799734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75284114-A-G

34799977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75284349-T-C

34800040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75284412-C-T

http://identifiers.org/hco/22/GRCh38#34800043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75284415-C-A

34800043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75284415-C-T

34800377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75284777-C-T

34800545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75284942-A-G

34800781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75285167-C-G

34800788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75285174-G-A

34800913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75285268-C-G

http://identifiers.org/hco/22/GRCh38#34804092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75287731-C-A

34804168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75287804-C-T

34804184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75287820-C-T

34804498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75288496-G-A

34804690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75288689-C-T

34804824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75288726-C-T

34804979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75288882-A-T

34804995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75288898-C-G

34804995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75288898-C-T

34805014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75288917-T-A

34805017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75288920-G-T

34805028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75288931-A-G

34805028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75288931-A-T

http://identifiers.org/hco/22/GRCh38#34805110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75288997-C-A

34805938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75289551-C-T

34805945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75289558-C-G

34806574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290116-A-T

34806613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290155-T-C

34806652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290194-C-T

http://identifiers.org/hco/22/GRCh38#34806688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75290232-C-A

34806733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290283-A-G

34807038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290544-T-C

34807083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290588-A-G

34807160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290683-C-G

34807231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290755-C-T

34807312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290836-G-A

34807315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290840-C-T

34807347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75290861-C-G

34807508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75291006-G-T

34807683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75291272-A-G

34807768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75291359-A-G

34808928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75294723-A-G

34809040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75294818-T-C

http://identifiers.org/hco/22/GRCh38#34809054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75294832-A-C

http://identifiers.org/hco/22/GRCh38#34809167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75294944-A-C

34809174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75294951-G-A

34809226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75294991-C-T

34809328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75295091-T-C

34809521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75295273-C-T

34809559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75295297-T-C

34809578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75295316-G-A

34814071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75296444-G-C

34814122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75296495-A-G

34814240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75296637-G-A

34814240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75296637-G-T

34814281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75296684-G-A

34814744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75297112-A-G

34815173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75297121-A-G

34815277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75297222-G-C

34815463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75297387-T-C

34823814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75297709-G-A

34823900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75297800-G-T

34824084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75297975-G-A

34824220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75298092-T-G

34824264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75298145-C-T

34825389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75299939-A-G

34825405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75299947-A-G

34825513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300052-G-A

34825520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300059-T-C

34825838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300365-T-A

34825838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300365-T-C

34825878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300412-G-A

34826014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300524-G-A

34826035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300543-A-G

34826049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300557-T-C

34826059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300567-T-C

34826060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300568-G-A

34826110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75300616-T-C

34826494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75301231-A-G

34826641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75301429-C-G

34826641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75301429-C-T

34827049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75301828-T-C

34827838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75302995-G-A

34827843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75303000-G-A

34827847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75303004-A-G

34833050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75306096-A-T

34833090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75306140-T-G

34833428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75306446-G-A

http://identifiers.org/hco/22/GRCh38#34833724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75306692-C-A

34833724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75306692-C-T

34833870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75306830-C-T

34842074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75307263-A-G

34842218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75307404-C-T

34842418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75307604-C-T

34842513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75307687-A-T

34842566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75307740-A-T

34842584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75307758-C-G

http://identifiers.org/hco/22/GRCh38#34842614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#75307789-C-A

34845931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75308513-T-C

34846210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75308661-C-T

34852101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75315631-T-C

34852168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75315690-G-A

34852212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75315732-T-C

34852297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75315817-C-G

http://identifiers.org/hco/22/GRCh38#34855156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75321645-A-C

34860108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75328414-C-T

34860115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75328421-A-T

34861032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329335-A-T

34861115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329412-T-G

34861338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329458-T-C

34861695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329656-C-T

34861987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75329948-A-G

http://identifiers.org/hco/22/GRCh38#34862133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75330045-C-A

34862202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75330106-G-A

34862272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75330176-G-A

34862542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75333195-G-A

http://identifiers.org/hco/22/GRCh38#34862569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75333222-C-A

34862794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75333401-A-G

34863334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75333650-A-G

34863537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75333876-C-T

http://identifiers.org/hco/22/GRCh38#34863726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75334048-C-A

34863794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334128-T-C

34863836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334169-G-A

34863882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334226-T-C

34863900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75334232-C-T

34864553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75337154-G-A

34864696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75337297-T-C

34864790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75337395-A-G

34868591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75341566-G-T

34868737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75341678-T-C

http://identifiers.org/hco/22/GRCh38#34869041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75341987-C-A

34869092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75342047-C-G

34869092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75342047-C-T

34869149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75342094-C-T

http://identifiers.org/hco/22/GRCh38#34869185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75342129-A-C

34869188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75342132-C-T

34869205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75342189-A-G

34869216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75342200-G-A

34869390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75342435-G-T

34869470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75342539-C-G

34869489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75342560-A-G

34870236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75343190-G-A

34870949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75345547-C-T

http://identifiers.org/hco/22/GRCh38#34870959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75345557-C-A

34871006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75346187-G-A

34871269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75347373-A-G

34871281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75347377-C-G

34871281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75347377-C-T

34871399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75347487-G-A

34871647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75347706-C-T

34871654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75347715-T-G

34872941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75349334-C-T

34873028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75349419-C-T

34874354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75351509-G-A

http://identifiers.org/hco/22/GRCh38#34874434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75351593-C-A

34874434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75351593-C-T

34874675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75351805-C-T

http://identifiers.org/hco/22/GRCh38#34874850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75352357-A-C

34874850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75352357-A-G

34874995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75352510-G-A

http://identifiers.org/hco/22/GRCh38#34875152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75352635-A-C

34875427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75352825-G-T

34875765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75353195-C-T

34875795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75353226-T-C

34875812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75353232-G-C

34875886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75353284-A-T

34876001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75353394-G-A

34879046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75356474-G-C

34879086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75356514-A-G

34881455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75356789-C-G

34881974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75357507-G-C

34882004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75357537-G-T

34882111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75357631-A-G

http://identifiers.org/hco/22/GRCh38#34882190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75357692-C-A

34882543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75358011-C-T

34882791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75358704-G-A

http://identifiers.org/hco/22/GRCh38#34882803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75358716-C-A

34882868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75358778-A-G

34882878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75358785-A-G

34883023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75358912-G-A

34883030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75358921-G-T

34883047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75358938-G-T

http://identifiers.org/hco/22/GRCh38#34883120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75359020-C-A

34883120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75359020-C-T

34883155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75359052-G-C

34883159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75359056-C-T

34883240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75359135-C-G

34883392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75359351-G-C

34883392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75359351-G-T

34883416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75359375-G-A

34883599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75359538-G-A

http://identifiers.org/hco/22/GRCh38#34883773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75359709-A-C

34883942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75359820-G-C

34883995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75359862-G-A

34883995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75359862-G-T

34884080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75359956-G-A

34884099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75359973-C-T

34884172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75360017-G-A

34884199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75360044-C-G

34884267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75360111-G-A

34884303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75360148-A-G

34884320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75360170-G-A

34884795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75360313-C-T

34884901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75360409-A-G

34884917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75360422-C-T

34885195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75360658-G-A

34885435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75360868-T-C

34885561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75360981-G-A

http://identifiers.org/hco/22/GRCh38#34885895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75361322-C-A

34891357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75365775-G-A

34891357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75365775-G-C

34891375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75365793-C-T

34891377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75365795-G-A

34891634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75366044-T-A

34891644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75366053-T-C

34891656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75366065-C-T

34891728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75366137-G-A

34891799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75366201-C-T

34891835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75366240-T-C

34891895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75366301-G-A

34891949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75366352-T-C

34892100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75366791-C-G

34892161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75366824-T-C

34892161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75366824-T-G

34892533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75367356-T-C

http://identifiers.org/hco/22/GRCh38#34903914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75370313-C-A

34904105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75370507-A-G

34904440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75370786-C-T

34904832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75371169-G-A

34906209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75371457-C-T

34906710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75371952-A-T

34907819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75373173-G-C

34907819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75373173-G-T

34908849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75374014-G-A

34909047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75374173-G-A

34909425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75374962-C-T

34909474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75375140-T-C

http://identifiers.org/hco/22/GRCh38#34909622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75375284-C-A

34909863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75375470-T-C

34910030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75375602-G-A

34910427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75376014-T-C

34910885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75376658-G-A

34911172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75376882-A-G

http://identifiers.org/hco/22/GRCh38#34911872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75377537-A-C

34911922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75377582-T-A

http://identifiers.org/hco/22/GRCh38#34912003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75377663-A-C

34912012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75377672-G-A

34912481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75384417-G-A

http://identifiers.org/hco/22/GRCh38#34912537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75384469-C-A

34913363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75385983-C-G

34913868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75386484-T-G

34914010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75386601-C-T

34914150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75386747-A-G

34914165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75386766-G-A

34914319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75386929-T-A

http://identifiers.org/hco/22/GRCh38#34914540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75387139-C-A

34914540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75387139-C-G

34914572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75387171-A-G

34914668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75387263-T-C

34914782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75387381-C-T

34915000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75387603-G-A

34915870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75394957-G-A

34916031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75395088-G-A

34916077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75395129-G-A

34917687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75395357-T-A

34917691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75395361-C-T

34917741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75395408-C-T

34918171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75395839-G-C

34918186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75395849-G-A

34918279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75395903-G-C

34918382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75396001-A-G

34918790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75396321-G-A

34919051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75396674-G-A

34919051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75396674-G-C

34919051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75396674-G-T

http://identifiers.org/hco/22/GRCh38#34919183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75396782-C-A

34919188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75396787-T-G

34919644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75397221-G-A

34919650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75397227-G-A

34919795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75397380-T-C

34919796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75397381-T-C

34920004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75397552-G-C

34920005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75397553-G-C

34920330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75398232-C-T

34920361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75398263-A-T

34920362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75398264-T-C

34920406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75398303-T-C

34920448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75398360-T-C

34920474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75398390-G-C

http://identifiers.org/hco/22/GRCh38#34920547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75398461-A-C

34920620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75398535-C-T

34920842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75398735-G-A

34920842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75398735-G-T

http://identifiers.org/hco/22/GRCh38#34925172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75399353-C-A

34925172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75399353-C-T

34925323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75399497-G-A

34929113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75401558-C-G

http://identifiers.org/hco/22/GRCh38#34929191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75401629-C-A

34929191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75401629-C-T

34929544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75401907-G-A

34929544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75401907-G-T

34929769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75401984-C-T

34929877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75402054-G-A

34929937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75402114-A-T

34930197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75402330-G-T

34930357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75402559-C-T

34930785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75402995-G-A

http://identifiers.org/hco/22/GRCh38#34930979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75403160-C-A

34930989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75403170-C-T

34931310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75403477-T-C

34931311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75403478-G-A

34931484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75403647-T-C

34931538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75403698-G-A

34932030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75404471-C-T

34932076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75404515-G-A

34932076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75404515-G-T

34932086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75404523-T-A

34932522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75411090-T-C

http://identifiers.org/hco/22/GRCh38#34932598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75411152-A-C

34932657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75411220-G-A

http://identifiers.org/hco/22/GRCh38#34932718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75411283-A-C

34932785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75411338-C-T

34934243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75411993-G-T

34934266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75412016-C-G

34934268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75412018-C-T

34934460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75412215-G-T

34934640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75412394-G-A

34934643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75412397-C-G

34934774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75412533-G-C

34934774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75412533-G-T

34939763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75413989-C-T

34940331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75414213-C-T

34940376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75414252-C-T

34940524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75414422-T-C

34940534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75414434-T-G

34940971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75414797-T-A

34941926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75415058-C-T

34941992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75415116-T-G

34942051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75415169-T-C

34942051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75415169-T-G

34942350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75415391-T-G

34942583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75415632-G-C

34942701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75415727-T-C

34942868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75415906-G-A

34942931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75415967-T-C

34943004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75417183-C-T

34943088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75417281-G-A

34943173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75417348-G-T

34943308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75417436-C-G

34943370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75417511-T-C

34943424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75417539-A-G

34943739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75417791-C-G

34943948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75417969-T-A

34944003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75418019-G-A

34944010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75418026-G-A

34944266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75418281-G-A

34944287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75418298-C-T

34944425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75418411-G-C

34944425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75418411-G-T

34944569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75418542-G-A

34944606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75418574-T-A

34944606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75418574-T-C

34944799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75418753-C-T

34950477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75423868-A-G

34950553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75423942-G-A

34950553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75423942-G-C

34950601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75423990-G-A

34950601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75423990-G-T

34950687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75424039-T-C

34950893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75424238-C-G

34950954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75424323-A-G

34950992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75424356-T-A

34950992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75424356-T-C

34950992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75424356-T-G

http://identifiers.org/hco/22/GRCh38#34951745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75425707-A-C

http://identifiers.org/hco/22/GRCh38#34951892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75425869-C-A

34951902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75425879-T-C

34951909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75425886-G-A

http://identifiers.org/hco/22/GRCh38#34951996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75425971-C-A

34952003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75425978-T-C

34962092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75463571-C-T

34962124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75463603-C-T

34962329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75463788-T-C

34962379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75463817-T-A

34962411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75463841-C-T

34962545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75463981-G-A

34962799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464329-C-T

34962955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464486-G-A

34962955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464486-G-T

34963204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75464680-G-A

34965083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75485708-C-T

34965719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75486137-C-T

34965800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75486216-A-G

34965939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75486345-A-G

34966416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75486516-T-C

34966900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75488218-T-C

34967069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75488378-G-A

34967076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75488383-G-C

34967443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75488865-T-A

34967443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75488865-T-C

34967601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75488971-G-T

34967783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75489791-C-T

http://identifiers.org/hco/22/GRCh38#34967978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75489964-A-C

34968010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75489996-T-C

34968070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75490058-A-G

34968802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75490682-C-T

http://identifiers.org/hco/22/GRCh38#34968861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75490740-C-A

34969015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75490893-T-C

http://identifiers.org/hco/22/GRCh38#34969072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75490950-A-C

34969102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75490981-T-A

34969102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75490981-T-C

34969170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75491051-C-T

34969204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75491081-A-G

34969460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75491414-T-C

34969696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75491643-A-G

34969953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75491900-T-C

34969981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75491935-G-A

34970055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75492000-C-T

34970287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75492226-T-C

34970287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75492226-T-G

34970294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75492238-G-A

34971466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75496408-G-A

34971607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75496536-G-A

34971793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75496723-C-G

34975553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75497767-G-T

34975879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75498075-T-A

34975879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75498075-T-C

34976887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75502094-G-A

34976922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75502126-G-A

34976989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75502192-G-A

34977079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75502282-T-C

34977374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75502564-C-G

34978814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75507137-A-G

34978840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75507163-G-T

34978870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75507190-G-A

34979000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75507333-G-T

34979676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75507616-G-A

34979676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75507616-G-C

34980133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75508063-C-T

34980384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75508278-A-G

http://identifiers.org/hco/22/GRCh38#34981615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75508958-C-A

34981669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75509011-G-A

34982487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75510262-C-T

34982490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75510265-C-T

34982516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75510291-A-T

34982548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75519118-C-T

http://identifiers.org/hco/22/GRCh38#34982664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#75519223-A-C

34982664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75519223-A-T

34982736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75519289-A-G

34983209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75519740-C-G

34983261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75519789-G-A

34983403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75519936-C-G

34983578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75520134-T-C

34983609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75520164-G-A

34983650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75520188-G-A

34983699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75520235-A-G

34983800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41188
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75520322-C-T