15760141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32922032-G-A

15760141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32922032-G-T

15760183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32921999-G-A

15760183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32921999-G-C

15760183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32921999-G-T

http://identifiers.org/hco/19/GRCh38#15760194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32921988-A-C

15760194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32921988-A-G

15760194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32921988-A-T

http://identifiers.org/hco/19/GRCh38#15760202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32921980-A-C

15760202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32921980-A-T

15760259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32921922-T-C

15760397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32921784-G-A

15760397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32921784-G-T

15760400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32921781-A-G

15760435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921743-G-A

15760435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921743-G-C

15760435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921743-G-T

http://identifiers.org/hco/19/GRCh38#15760440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32921738-C-A

15760440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921738-C-T

15760444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921734-G-A

15760444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921734-G-T

15760466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921713-T-G

http://identifiers.org/hco/19/GRCh38#15760492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32921677-C-A

15760492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921677-C-T

15760497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921672-G-A

15760497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921672-G-C

15760497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921672-G-T

15760514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921655-A-G

15760524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921645-G-A

15760524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921645-G-T

15760554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921614-G-T

http://identifiers.org/hco/19/GRCh38#15760559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32921609-C-A

15760559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921609-C-G

15760559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921609-C-T

15760564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921604-T-A

15760564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921604-T-C

15760564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921604-T-G

15760565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921603-G-A

15760565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921603-G-T

15760588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921576-T-C

15760685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921507-G-A

15760685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921507-G-T

http://identifiers.org/hco/19/GRCh38#15760733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32921462-C-A

15760733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921462-C-T

15760757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921440-C-T

http://identifiers.org/hco/19/GRCh38#15760765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32921436-A-C

15760765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32921436-A-G

http://identifiers.org/hco/19/GRCh38#15760873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32921328-A-C

15760873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32921328-A-G

15760873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32921328-A-T

15760928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921289-G-A

15760957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921270-A-G

15760979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921252-G-A

15760979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921252-G-C

http://identifiers.org/hco/19/GRCh38#15760980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32921251-C-A

15760980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921251-C-G

15760980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921251-C-T

15760984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921247-G-A

15760984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921247-G-T

15760988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921243-T-G

15761001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921230-T-G

15761004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921227-T-G

http://identifiers.org/hco/19/GRCh38#15761026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32921207-A-C

15761026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921207-A-G

15761026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921207-A-T

15761048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921189-A-G

15761048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921189-A-T

15761078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32921169-G-A

15761078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32921169-G-C

15761078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32921169-G-T

15761183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921070-T-A

15761183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32921070-T-C

http://identifiers.org/hco/19/GRCh38#15761207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32921042-A-C

15761207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 32921042-A-G

15761207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 32921042-A-T

http://identifiers.org/hco/19/GRCh38#15761280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32920971-C-A

15761280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32920971-C-T

http://identifiers.org/hco/19/GRCh38#15761390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32920860-C-A

15761390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32920860-C-T

15761391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32920859-A-G

15761428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32920827-T-C

http://identifiers.org/hco/19/GRCh38#15761430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32920825-C-A

15761430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32920825-C-T

http://identifiers.org/hco/19/GRCh38#15761433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32920822-C-A

15761433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32920822-C-G

15761433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32920822-C-T

15761434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32920821-T-C

15769436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32919424-A-G

15769485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32919402-G-T

15769600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32919291-G-A

15769600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32919291-G-T

http://identifiers.org/hco/19/GRCh38#15769627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32919264-A-C

15769657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32919234-G-C

15769693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32919198-C-T

15769715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32919176-C-T

15769720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 32919171-G-T

15769747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32919144-G-A

15769747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32919144-G-T

http://identifiers.org/hco/19/GRCh38#15769791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32919100-C-A

15769791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32919100-C-G

15769791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32919100-C-T

15769805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32919086-G-A

15769805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32919086-G-T

15769825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32919060-C-T

15769835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32919045-T-A

15769835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32919045-T-C

15769835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32919045-T-G

http://identifiers.org/hco/19/GRCh38#15769840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#32919041-C-A

http://identifiers.org/hco/19/GRCh38#15769875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32919007-C-A

15769875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32919007-C-T

15769902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32918980-G-A

15769902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32918980-G-T

http://identifiers.org/hco/19/GRCh38#15770109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32918806-C-A

15770109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32918806-C-G

15770464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32917952-C-G

15770464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32917952-C-T

15770549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32917856-C-T

15770723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32917685-C-T

15770725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32917683-T-C

15770802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32917617-G-A

15770802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32917617-G-T

15770848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32917573-A-G

15771031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32916970-G-A

15771052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32916949-A-T

15771055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32916946-A-G

15771062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32916938-G-A

15771140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32916860-G-A

15771204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32916796-T-A

15771204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32916796-T-G

15771293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32916707-C-G

15771293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32916707-C-T

15771296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32916704-A-G

15771305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32916695-C-T

15771347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32916680-A-G

15771392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32916635-G-T

15771586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32916462-C-T

15771654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32916406-C-T

15771882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914514-A-G

http://identifiers.org/hco/19/GRCh38#15771898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32914498-C-A

15771898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914498-C-T

15771905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914488-T-C

15771905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914488-T-G

http://identifiers.org/hco/19/GRCh38#15771924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32914482-A-C

15771924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914482-A-G

http://identifiers.org/hco/19/GRCh38#15771938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32914464-C-A

15771938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914464-C-T

http://identifiers.org/hco/19/GRCh38#15771939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32914463-C-A

http://identifiers.org/hco/19/GRCh38#15771943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32914459-A-C

15771943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914459-A-G

15771947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914455-T-C

http://identifiers.org/hco/19/GRCh38#15771948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32914454-A-C

15771948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914454-A-G

15771948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914454-A-T

http://identifiers.org/hco/19/GRCh38#15771949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32914453-C-A

15771949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914453-C-G

15771949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914453-C-T

15771960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914441-T-G

15771974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914427-C-T

http://identifiers.org/hco/19/GRCh38#15771978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32914423-C-A

15771978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914423-C-T

15772027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914376-G-T

http://identifiers.org/hco/19/GRCh38#15772243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32914167-C-A

15772243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914167-C-G

15772243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914167-C-T

http://identifiers.org/hco/19/GRCh38#15772244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32914166-A-C

15772291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914109-G-T

15772324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914078-A-G

15772325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914077-T-A

15772325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32914077-T-C

15772423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913974-C-G

15772447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913955-T-G

15772676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32913389-G-A

15772676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32913389-G-T

15772803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32913261-G-C

http://identifiers.org/hco/19/GRCh38#15773089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32913016-C-A

15773091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32913014-G-A

http://identifiers.org/hco/19/GRCh38#15774020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32911699-C-A

15774020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911699-C-T

http://identifiers.org/hco/19/GRCh38#15774025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32911694-C-A

15774025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911694-C-T

15774042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911678-C-T

http://identifiers.org/hco/19/GRCh38#15774174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32911546-C-A

15774174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32911546-C-T

15774228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911495-C-G

http://identifiers.org/hco/19/GRCh38#15774232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32911491-C-A

15774232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911491-C-T

15774247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911475-A-G

15774266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911458-T-C

15774273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911451-C-T

15774380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911345-A-G

http://identifiers.org/hco/19/GRCh38#15774390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32911334-C-A

http://identifiers.org/hco/19/GRCh38#15774398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32911322-A-C

15774398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911322-A-G

http://identifiers.org/hco/19/GRCh38#15774401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32911319-C-A

15774453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911265-G-A

15774453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911265-G-T

15774483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911235-G-A

15774483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911235-G-C

15774483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911235-G-T

15774554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911198-C-T

15774571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911181-A-G

15774731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32911045-G-T

15774803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32910971-G-C

15774803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32910971-G-T

15774970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32910827-G-A

15775020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32910780-G-C

http://identifiers.org/hco/19/GRCh38#15776269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32909865-C-A

15776269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909865-C-G

15776269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909865-C-T

15776272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909862-T-A

15776272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909862-T-G

15776299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909835-T-A

15776299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909835-T-C

15776340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909804-G-A

15776340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909804-G-C

15776340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909804-G-T

http://identifiers.org/hco/19/GRCh38#15776381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32909777-A-C

15776395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909763-T-C

http://identifiers.org/hco/19/GRCh38#15776424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32909734-A-C

15776424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32909734-A-G

15776447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32909711-G-T

15776621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909545-G-C

15776621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909545-G-T

http://identifiers.org/hco/19/GRCh38#15776622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32909541-A-C

15776622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909541-A-G

15776671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909484-T-C

15776671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909484-T-G

http://identifiers.org/hco/19/GRCh38#15776688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32909465-C-A

15776700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909453-G-T

15776708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32909445-C-T

15777324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32906393-T-C

http://identifiers.org/hco/19/GRCh38#15777597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32905812-C-A

15777597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32905812-C-T

15777664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32905746-G-A

http://identifiers.org/hco/19/GRCh38#15777804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32905601-C-A

15777824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32905583-G-A

http://identifiers.org/hco/19/GRCh38#15779624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32905308-C-A

15779624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32905308-C-G

15779624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32905308-C-T

http://identifiers.org/hco/19/GRCh38#15779677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32905267-C-A

15779677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32905267-C-G

15779677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32905267-C-T

15779920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32905023-G-A

15779920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32905023-G-C

15779920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32905023-G-T

15779956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32904988-G-A

15779956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39945
most severe consequence: non coding transcript exon variant
orthologous variants: 32904988-G-T