128459591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32668306-G-T

128459942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667935-T-C

128459944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667933-C-T

128459979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667903-G-T

128459989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667893-T-A

128460088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667795-A-G

128460200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667734-A-G

128460419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667523-A-G

128460511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667453-C-T

http://identifiers.org/hco/11/GRCh38#128460535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32667428-C-A

128460535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667428-C-G

128460584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667396-A-G

128460739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667252-G-A

128460739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667252-G-T

128460789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667202-A-G

128460868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667128-T-C

http://identifiers.org/hco/11/GRCh38#128460898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32667096-C-A

128461009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32667026-T-G

http://identifiers.org/hco/11/GRCh38#128461046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32666989-C-A

128461154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32666886-G-A

128461154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32666886-G-T

128461160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32666880-G-A

128461160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32666880-G-T

128461354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32666689-T-C

128461483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32666560-T-C

128461822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32666245-C-T

128461854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32666217-A-G

128461995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32666112-G-T

http://identifiers.org/hco/11/GRCh38#128462191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32665903-C-A

http://identifiers.org/hco/11/GRCh38#128462221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32665874-C-A

128462221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32665874-C-T

128462223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 3 prime UTR variant
orthologous variants: 32665872-G-T

http://identifiers.org/hco/11/GRCh38#128462865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32664730-C-A

128462865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32664730-C-T

128463010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32664594-T-C

128463207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32664456-C-T

128463336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32664371-T-A

http://identifiers.org/hco/11/GRCh38#128463376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32664328-C-A

128463384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32664321-G-A

128463384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32664321-G-T

http://identifiers.org/hco/11/GRCh38#128463491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32664229-A-C

128463491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32664229-A-G

128463510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32664210-T-A

128463510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32664210-T-C

128463632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32664088-A-G

http://identifiers.org/hco/11/GRCh38#128463715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32664008-C-A

128463715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32664008-C-T

128463786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32663937-A-G

128463798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32663933-T-C

128463798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32663933-T-G

128463844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32663880-T-C

128465400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32663407-G-A

128465671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32663148-T-C

128465778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32663051-G-A

128465894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32662901-C-T

128466582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32662347-T-C

128466619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32662323-A-G

128466659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32662296-C-T

128466993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32661892-C-T

128467123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32661748-C-T

128467287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32661619-G-A

128467287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32661619-G-C

128467376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32661549-T-C

128467459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32661475-C-T

128467914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: 32661054-C-T

128468097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32660889-C-T

128468699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32660056-T-C

http://identifiers.org/hco/11/GRCh38#128469006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32659544-A-C

128469006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32659544-A-G

128469169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32659371-C-T

128469720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32658859-C-T

128469907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32658668-G-A

128469962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32658615-A-G

128470390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32658381-C-T

128470438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32658343-T-C

128470602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32658198-T-C

http://identifiers.org/hco/11/GRCh38#128470624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32658179-A-C

128470703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32658124-G-T

128470755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32658072-C-T

http://identifiers.org/hco/11/GRCh38#128470841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32657991-A-C

128470865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657970-T-C

128470912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657926-G-A

128471024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657836-C-T

128471044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657819-T-A

128471055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657808-C-T

128471140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657765-G-C

128471259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657662-G-A

128471375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657555-C-G

128471513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657400-G-A

128471558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657351-A-G

128471717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657195-T-C

128471719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657188-C-T

128471795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657105-T-C

128471823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657089-T-G

128471842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32657076-T-C

128472007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32656920-C-T

128472012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32656915-A-G

128472012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32656915-A-T

128472091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32656829-T-C

128472096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32656824-G-T

128472152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32656769-C-T

128472793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32656144-C-T

128473192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32655771-G-C

128473254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32655732-A-G

128473382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32655628-C-T

128473902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32655159-T-C

128473942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32655120-G-A

128474270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32654827-G-C

128474475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32654633-C-T

128474592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32654519-T-C

128474654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32654448-G-A

128474654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32654448-G-C

128474930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32654199-A-T

128475061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32654000-C-T

128475091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32653975-T-A

128475169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32653883-C-T

128475221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32653827-C-G

http://identifiers.org/hco/11/GRCh38#128475226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32653821-A-C

128475270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32653778-A-G

128475365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32653686-T-C

http://identifiers.org/hco/11/GRCh38#128476459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32653006-A-C

128476538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32652931-A-G

128476858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32652561-T-G

128476895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32652515-C-T

128476905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32652505-A-T

128477208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32652168-T-C

128477613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32651805-C-G

128477677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32651749-C-T

http://identifiers.org/hco/11/GRCh38#128477702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32651724-A-C

128477743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32651669-T-C

128477902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32651521-C-T

128478924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32650896-T-A

128478924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32650896-T-C

128478981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32650832-C-T

128479278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32650562-T-A

128479315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32650527-T-G

128479471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32650375-G-A

128479669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32650143-G-A

http://identifiers.org/hco/11/GRCh38#128479720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32650102-C-A

128479720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32650102-C-T

128479731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32650091-C-T

128479987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32649836-A-T

128480012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32649811-G-A

128480043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32649784-A-G

128480060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32649767-G-A

128480060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32649767-G-C

http://identifiers.org/hco/11/GRCh38#128480173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32649671-C-A

128480250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, missense_variant
orthologous variants: 32649594-C-T

128480560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32649286-G-T

128480684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32649172-G-C

128480795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32649063-T-C

128480966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32648898-C-T

128480984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32648880-C-T

128481197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32648679-T-C

128481228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32648656-G-A

128481233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32648651-A-T

128481235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32648649-T-C

128481235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32648649-T-G

128481314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32648570-T-A

http://identifiers.org/hco/11/GRCh38#128481575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32648314-C-A

128481830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32648091-T-C

http://identifiers.org/hco/11/GRCh38#128481916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32648033-C-A

128482001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32647968-T-C

http://identifiers.org/hco/11/GRCh38#128482048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32647924-C-A

128482063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32647919-C-T

128482530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32647568-G-A

128482679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32647431-C-T

128482743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32647372-T-C

128482806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32647310-G-A

128483194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32646948-C-T

128483515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32646631-C-T

128483602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32646544-G-A

128483602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32646544-G-C

128483796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32646392-G-A

128484087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32646174-G-C

128484101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32646160-T-C

http://identifiers.org/hco/11/GRCh38#128484249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32646014-C-A

128484625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32645670-C-T

128484676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32645619-T-C

128484776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32645527-G-T

128485191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32645112-T-A

128485191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32645112-T-C

128485199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32645104-A-T

128485221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32645084-T-A

128485221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32645084-T-C

128485223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32645081-G-A

128485223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32645081-G-T

128485414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32644890-T-C

128485509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32644788-G-C

128485655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32644685-C-T

128485747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32644592-T-A

128485747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32644592-T-G

128485941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32644452-A-G

128485941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32644452-A-T

128486052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32644344-G-A

128486052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32644344-G-T

http://identifiers.org/hco/11/GRCh38#128486203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32644187-C-A

128486203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32644187-C-T

http://identifiers.org/hco/11/GRCh38#128486231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32644158-A-C

128486235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32644154-A-G

128486241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32644148-A-T

128486334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32644055-T-C

128486454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32643933-C-T

128486695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32643679-G-A

128486706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32643668-G-A

http://identifiers.org/hco/11/GRCh38#128486820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32643573-A-C

128486844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32643553-A-G

128487148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32643240-G-C

128487183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32643201-C-T

http://identifiers.org/hco/11/GRCh38#128487191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32643193-A-C

128487233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32643151-G-T

128487262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32643123-T-C

128487274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32643111-A-G

128488159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32642638-C-T

128488458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32642364-G-A

http://identifiers.org/hco/11/GRCh38#128488459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32642363-C-A

128488459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32642363-C-G

128488459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32642363-C-T

128488630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32642192-G-A

128488664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32642158-T-C

128488811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32642006-T-A

128488894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32641929-C-T

128488982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32641842-C-T

http://identifiers.org/hco/11/GRCh38#128489068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32641760-A-C

http://identifiers.org/hco/11/GRCh38#128489158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32641685-C-A

128489158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32641685-C-T

128489219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32641616-G-A

128489219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32641616-G-T

128489454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, stop_gained
orthologous variants: 32641385-C-T

128489568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32641291-G-A

128489578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32641281-T-C

128489583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32641276-G-A

128489704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32641173-G-A

128489801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32641083-T-C

128489940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32640924-T-C

http://identifiers.org/hco/11/GRCh38#128490107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32640813-C-A

128490159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32640760-G-T

128490685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32639848-G-A

128490685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32639848-G-T

128491184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32639638-T-C

128491294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32639543-G-C

128491355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32639481-C-T

128491366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32639474-G-A

128491539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32639321-C-T

128491629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32637488-C-T

128491669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32637450-G-A

128491702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32637416-C-T

128491845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32637293-G-A

http://identifiers.org/hco/11/GRCh38#128491940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32637229-C-A

128491942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32637227-G-A

128492200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32637002-G-A

128492237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32636907-C-T

128492477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32636693-A-G

128492502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32636668-G-A

http://identifiers.org/hco/11/GRCh38#128492555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32636618-A-C

128492673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32636478-G-A

128492802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32636352-T-A

128492836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32636318-T-C

128493200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32635966-G-C

128493371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32635796-G-A

128493391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32635776-T-C

128493554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32635638-A-G

128493691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32635507-G-A

http://identifiers.org/hco/11/GRCh38#128493812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32635382-C-A

128493885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32635321-G-C

http://identifiers.org/hco/11/GRCh38#128493925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32635282-A-C

128493978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32635188-A-G

128494370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32634829-A-G

128494411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32634750-G-A

128494429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32634741-C-G

128494429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32634741-C-T

128494959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32634215-T-A

128494962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32634212-G-A

128495167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32634111-G-T

128495237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32634042-G-A

128495870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32633407-A-G

http://identifiers.org/hco/11/GRCh38#128496008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32633304-C-A

128496008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32633304-C-T

128496009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32633303-G-A

128496242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32633079-C-T

128496336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32632981-G-A

128496375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32632935-T-A

128496552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32632801-G-A

128496631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32632732-T-C

128496675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32632694-C-T

http://identifiers.org/hco/11/GRCh38#128496844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32632533-C-A

128497045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32632385-T-C

128497078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: 32632351-A-G

128497087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: 32632335-C-T

http://identifiers.org/hco/11/GRCh38#128497158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32632269-A-C

http://identifiers.org/hco/11/GRCh38#128497291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32632150-A-C

http://identifiers.org/hco/11/GRCh38#128497292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32632149-A-C

128497292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: 32632149-A-G

128497379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: 32632055-G-A

128497486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32631974-C-G

128497522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32631938-G-T

128497523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32631937-G-C

128497523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32631937-G-T

128497576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 32631884-G-T

128497656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 32631804-G-T

128497659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 32631801-G-A

128497659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 32631801-G-T

http://identifiers.org/hco/11/GRCh38#128497771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32631688-C-A

128498576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32630943-C-T

128498787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32630718-G-T

128499048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32630370-C-T

128499053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32630360-G-A

128499053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32630360-G-C

128499053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32630360-G-T

128499071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32630342-C-G

128499071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32630342-C-T

128499143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32630263-A-G

128499428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32629993-T-A

128499721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32629736-C-T

128499728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32629700-C-T

128499729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32629699-A-G

128499735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32629693-C-T

128500262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32629294-A-G

128500354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32629215-A-G

128500377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32629191-T-A

128500412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32629156-T-C

http://identifiers.org/hco/11/GRCh38#128500788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32628791-C-A

128501135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32628459-C-T

128501136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32628458-G-A

128501402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32628246-T-A

128501402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32628246-T-C

128501734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 32627927-A-G

128501780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32627881-C-T

128501802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32627859-T-A

128501815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32627846-C-T

128501864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32627798-G-C

128501873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32627791-C-G

128501957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32627717-C-T

128502002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32627676-G-A

128502134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32627573-C-T

128502382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32627348-T-A

128502479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32627285-T-G

128502561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32627202-A-G

128502651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32627038-G-A

128503094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 32626595-A-G

128503328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32626396-C-T

128503341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32626391-C-G

http://identifiers.org/hco/11/GRCh38#128503510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32626235-A-C

128504075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32625665-G-A

128504234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32625500-G-A

128504293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32625451-G-A

128504715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32625048-T-C

128504732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32625031-C-T

128505147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32624627-G-T

http://identifiers.org/hco/11/GRCh38#128505161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32624607-C-A

128505241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32624543-A-G

128505309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32624477-A-G

http://identifiers.org/hco/11/GRCh38#128505389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32624399-C-A

128505389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32624399-C-T

128505393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32624395-T-A

128505440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32624346-A-G

128505459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32624328-A-T

128505777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32624024-A-G

128505777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32624024-A-T

128505800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32623998-C-G

128505950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32623840-G-C

128506147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32623652-T-C

128506543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32623320-G-A

128506543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32623320-G-C

128506779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32623134-G-A

128506834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32623094-A-G

128507129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 32622826-G-A

128507290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32622672-G-C

128507653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32622314-A-G

128507753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32622229-G-A

128508775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32621315-G-A

http://identifiers.org/hco/11/GRCh38#128508783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32621307-A-C

128508784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32621306-A-G

128508824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32621273-T-C

128508840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32621257-T-C

128508955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32621131-T-C

128509059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32621030-G-A

128509059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32621030-G-C

128509147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32620953-C-T

128509264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32620829-C-T

http://identifiers.org/hco/11/GRCh38#128509530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32620565-A-C

http://identifiers.org/hco/11/GRCh38#128509541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32620554-C-A

http://identifiers.org/hco/11/GRCh38#128509582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32620552-C-A

128509582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32620552-C-T

http://identifiers.org/hco/11/GRCh38#128509598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32620541-C-A

128509598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32620541-C-T

128509602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32620537-A-G

128509631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32620509-C-T

128509632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32620508-G-A

128509998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32620168-C-T

128510108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32620057-T-C

128510167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32619989-A-G

128510353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32619807-G-A

128510485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32619695-G-A

128510792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32619372-A-G

128511009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32619124-C-T

128511353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32618756-C-T

http://identifiers.org/hco/11/GRCh38#128512063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32618193-C-A

128512063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32618193-C-T

128512270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32617995-A-G

128512316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32617929-G-A

128512366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32617863-G-A

128512650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32617540-C-G

128512650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32617540-C-T

http://identifiers.org/hco/11/GRCh38#128512879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32617312-A-C

128512996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32617192-G-A

128513119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32617030-C-G

128513519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32616360-G-C

128513630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32616262-A-G

128513910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32616154-A-G

128513971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32616092-G-A

128514348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32615301-C-T

128514607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32614898-A-G

128514896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32614630-C-G

128514896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32614630-C-T

128515053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32614498-T-C

128515278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32614251-G-A

128515286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32614243-A-G

128515288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32614241-T-C

128515501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32614013-C-T

128515538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32613995-A-G

http://identifiers.org/hco/11/GRCh38#128515848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32613696-A-C

128516247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32613324-A-G

128516333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32613240-C-T

128516401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32613172-C-T

128516412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32613161-G-C

128516496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32613081-G-A

128516496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32613081-G-T

http://identifiers.org/hco/11/GRCh38#128516577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32613004-C-A

128516776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32612856-T-C

128516787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32612839-T-C

128516892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32612745-T-C

128516996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32612662-G-A

128516996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32612662-G-C

128517097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32612563-G-A

128517120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32612540-C-T

128517266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32612448-A-G

128518396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32611354-T-C

128518499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32611265-T-C

128518665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32611108-C-T

http://identifiers.org/hco/11/GRCh38#128518760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32611012-A-C

128518964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32610799-G-C

128519200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32610580-A-T

128519580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32610186-T-C

128519725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32610048-G-A

128519736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32610037-C-T

http://identifiers.org/hco/11/GRCh38#128519784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32609991-C-A

128520066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32609491-A-G

128520732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32608841-C-T

128520734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32608839-T-C

128521353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32608265-A-G

128521456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32608152-A-G

http://identifiers.org/hco/11/GRCh38#128521544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32608059-C-A

128521597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32608005-C-T

128521702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607888-C-G

128521771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607842-T-A

128521771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607842-T-C

128521771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607842-T-G

http://identifiers.org/hco/11/GRCh38#128521804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32607826-C-A

128521888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607783-G-A

128521888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607783-G-T

http://identifiers.org/hco/11/GRCh38#128521899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32607773-C-A

128521899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607773-C-G

128521899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607773-C-T

128521901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607771-G-A

128521901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607771-G-T

128522026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32607644-A-G

128522077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32607591-G-C

128522077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32607591-G-T

128522103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32607576-T-C

http://identifiers.org/hco/11/GRCh38#128522110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32607569-C-A

http://identifiers.org/hco/11/GRCh38#128522304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32607380-C-A

128522304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32607380-C-G

128522304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32607380-C-T

128522307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32607377-T-C

128522307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 32607377-T-G

http://identifiers.org/hco/11/GRCh38#128522320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32607367-C-A

128522320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607367-C-T

http://identifiers.org/hco/11/GRCh38#128522323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32607364-C-A

128522323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607364-C-G

128522323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607364-C-T

http://identifiers.org/hco/11/GRCh38#128522371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32607320-C-A

128522371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: 32607320-C-G

http://identifiers.org/hco/11/GRCh38#128522378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32607313-C-A

128522449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32607254-G-A

128522538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607182-G-A

128522538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607182-G-T

128522542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607178-G-T

128522624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32607101-G-A

128522628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: 32607097-G-A

128522807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: 32606919-G-A

128522807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: 32606919-G-C

128522832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: 32606899-G-C

128522832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, undefined
orthologous variants: 32606899-G-T

128523106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32606653-C-T

128523217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32606550-G-A

128523456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32606339-C-T

128523520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32606271-T-G

128523521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32606270-T-A

128523631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32606164-G-C

128523652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32606134-G-A

128523716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32606063-T-A

128523716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32606063-T-G

128523761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32606001-G-A

http://identifiers.org/hco/11/GRCh38#128523918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32605853-C-A

128523986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32605800-C-T

128524113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32605689-T-C

128524190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32605614-T-C

128524244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32605556-G-C

128524258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32605542-T-C

128524487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32605354-T-C

128525164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32604760-A-G

128525259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32604706-T-C

128525637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32604377-A-T

128525758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32604241-A-G

128525794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32604209-C-T

128525951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32604057-G-T

128525954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32604054-T-C

128526161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32603845-G-T

128526166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32603840-G-A

128526166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32603840-G-T

128526245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32603787-T-C

128526255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32603777-T-C

128526276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32603755-A-G

128526291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32603740-C-T

128526313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32603719-C-T

http://identifiers.org/hco/11/GRCh38#128526334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32603702-C-A

128526334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32603702-C-T

128526350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32603686-T-C

128526377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32603659-G-A

128526393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32603643-G-T

128526410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32603634-A-T

http://identifiers.org/hco/11/GRCh38#128526425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32603619-C-A

http://identifiers.org/hco/11/GRCh38#128526491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32603564-C-A

128526491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32603564-C-T

128526726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32603344-T-C

128526729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32603341-A-T

128527089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32603151-G-A

128527101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32603139-G-A

128527152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32603106-T-C

128527154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32603104-G-A

http://identifiers.org/hco/11/GRCh38#128527246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32603014-A-C

128527246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32603014-A-G

http://identifiers.org/hco/11/GRCh38#128527336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32602925-C-A

128527451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32602804-G-C

128527451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32602804-G-T

128527462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32602793-C-T

128527514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32602736-G-A

128527514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32602736-G-T

http://identifiers.org/hco/11/GRCh38#128527540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32602699-C-A

128527791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32602469-C-T

128527885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32602376-G-A

128527973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32602284-A-G

http://identifiers.org/hco/11/GRCh38#128527996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32602220-C-A

128527998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32602218-A-G

128528240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32602004-G-T

http://identifiers.org/hco/11/GRCh38#128528412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32601843-C-A

128528529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32601732-G-A

128528809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32601494-G-A

128528814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32601489-G-C

128528899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32601389-T-C

128528945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32601339-C-T

128528946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32601338-G-A

128529300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32601014-G-A

128529345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32600979-G-C

128529379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32600945-G-A

128529494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32600839-G-A

128529494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32600839-G-T

128529514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32600819-A-G

128529816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32600595-G-A

128529991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32600475-T-C

128529991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32600475-T-G

128530135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 32600304-C-G

128530162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32600278-A-G

http://identifiers.org/hco/11/GRCh38#128530191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32600243-C-A

128530203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32600231-G-A

http://identifiers.org/hco/11/GRCh38#128530243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32600191-C-A

http://identifiers.org/hco/11/GRCh38#128530317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32600135-C-A

128530317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32600135-C-T

128530346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32600106-A-G

128530360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32600092-G-A

128530360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32600092-G-T

http://identifiers.org/hco/11/GRCh38#128530457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32600012-C-A

128530619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32599857-G-A

http://identifiers.org/hco/11/GRCh38#128530914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32599408-C-A

128531113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32599229-T-A

128531511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32598318-T-A

128531515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32598314-C-T

128531573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32598261-T-C

128531576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32598258-A-G

128531630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32598203-A-T

128531755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32598081-G-A

128532226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32597876-C-T

128532608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32597482-A-T

128532631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32597459-G-T

128532634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32597456-C-T

128533036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32597041-C-T

http://identifiers.org/hco/11/GRCh38#128533213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32596855-A-C

128533256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32596771-A-G

128533315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32596699-T-C

128533474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32596533-G-C

http://identifiers.org/hco/11/GRCh38#128533492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32596515-C-A

128533761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32596262-G-A

128533761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32596262-G-T

128533856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32596198-T-C

128533856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32596198-T-G

128533920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32596143-G-A

128534079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32595981-C-T

128534097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32595918-T-C

http://identifiers.org/hco/11/GRCh38#128534244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32595788-A-C

http://identifiers.org/hco/11/GRCh38#128534317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32595345-A-C

128534321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32595341-G-A

http://identifiers.org/hco/11/GRCh38#128535719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32594803-A-C

128535741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32594784-T-A

128535902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32594650-C-T

128535905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32594647-C-T

128535974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32594576-T-C

128535988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32594562-T-C

http://identifiers.org/hco/11/GRCh38#128536001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32594549-A-C

128536295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron variant
orthologous variants: 32594292-A-G

128536624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32593966-G-T

128536789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32593808-A-G

128537198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32593424-T-G

128537639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32593020-G-T

128537724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32592899-G-A

128537839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32592786-T-C

http://identifiers.org/hco/11/GRCh38#128537967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32592648-A-C

128538645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32591995-T-A

128538757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32591899-C-T

128538920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32591739-T-C

128538954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32591706-A-G

128539010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32591664-A-G

128539254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32591439-G-C

http://identifiers.org/hco/11/GRCh38#128539449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32591237-C-A

128539535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32591109-C-G

128539968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32590646-G-A

128540046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32590596-T-A

128540783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32589919-G-T

128541060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32589651-C-T

128543625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32588655-A-G

128543744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32588547-G-A

128543773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32588519-C-G

128543773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32588519-C-T

128543823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32588479-T-G

128544126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32587859-G-T

128544663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32587340-T-C

http://identifiers.org/hco/11/GRCh38#128544863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32587137-C-A

128545058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32586937-T-C

128545266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32586733-A-G

128545397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32586589-C-T

128545398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32586588-A-G

128545458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32586525-T-C

128545730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32586287-G-A

128545957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32586097-T-C

128547277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32585302-A-G

http://identifiers.org/hco/11/GRCh38#128547542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32584888-A-C

http://identifiers.org/hco/11/GRCh38#128547569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32584864-C-A

128547654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32584790-A-G

128547655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32584789-T-A

128547946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32584506-A-G

128548132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32584366-A-G

128548137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32584361-G-A

128548798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32584005-G-A

128548798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32584005-G-T

128548809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32583994-C-G

128548809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32583994-C-T

128549189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32583640-C-T

128549627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32583193-G-C

128549665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32583155-T-C

128549834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32583006-G-A

128549834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32583006-G-T

http://identifiers.org/hco/11/GRCh38#128550054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32582698-C-A

128550749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32582062-G-A

128550969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32581737-G-A

128551307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32581376-A-T

128551525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32581152-C-T

128551624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32581051-C-T

128551728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32580947-G-T

http://identifiers.org/hco/11/GRCh38#128552542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32580284-C-A

128552545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32580281-T-A

128552613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32580223-A-G

http://identifiers.org/hco/11/GRCh38#128552661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32580178-C-A

128552708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32580131-A-G

128552985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32579821-A-T

128552993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32579813-G-C

128553002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32579804-A-G

128553006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32579800-G-A

128553494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32579312-A-G

128553623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32579203-G-A

128553758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32579085-T-C

128554087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32578714-G-A

128554328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32578474-G-C

128554418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32578393-T-C

http://identifiers.org/hco/11/GRCh38#128554419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32578392-A-C

128554436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32578374-T-C

128554447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32578363-T-G

128555210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32577204-C-G

128555228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32577187-T-A

128555234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32577181-C-T

128555244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32577169-T-C

http://identifiers.org/hco/11/GRCh38#128555385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32577038-C-A

128555455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576964-T-C

128555836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576519-G-A

128555836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576519-G-C

128555884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576459-C-G

128555967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576382-A-T

128556148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576205-G-A

128556148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576205-G-T

128556149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576204-G-T

http://identifiers.org/hco/11/GRCh38#128556161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32576192-C-A

128556161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576192-C-T

128556189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576165-G-A

128556189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576165-G-C

128556189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576165-G-T

128556207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576148-G-A

128556207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576148-G-T

128556210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576145-A-G

http://identifiers.org/hco/11/GRCh38#128556231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32576131-A-C

128556232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576130-T-C

128556257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576105-T-C

128556268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576036-C-T

128556275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32576029-T-C

128556350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32575954-G-A

128556350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32575954-G-T

http://identifiers.org/hco/11/GRCh38#128556386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32575918-A-C

128556386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32575918-A-G

128556388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32575916-A-G

128556419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32575885-T-C

128556453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32575850-G-C

128556528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32575774-G-A

128556528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32575774-G-T

http://identifiers.org/hco/11/GRCh38#128556742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32575577-C-A

128556849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32575466-T-C

128556855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32575460-A-G

128556855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32575460-A-T

128556856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32575459-T-A

http://identifiers.org/hco/11/GRCh38#128556858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32575457-C-A

128556993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32575325-A-G

128557140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32575197-C-T

128557398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32574852-T-C

128559976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32572861-C-G

128560542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32572602-G-A

128560556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32572588-A-G

128560576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32572568-A-G

128560786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32572251-A-G

128561061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32570947-A-G

128561534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32570494-C-T

http://identifiers.org/hco/11/GRCh38#128561730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32570312-C-A

128561733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32570309-C-T

128561795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32570252-T-C

128562970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32569162-A-G

128563019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32569123-C-T

128563061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32569080-G-A

128563069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32569069-G-C

128563112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32569024-C-T

128563313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568866-T-A

128563313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568866-T-G

128563424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568761-A-G

http://identifiers.org/hco/11/GRCh38#128563700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32568490-C-A

128563744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568450-C-G

128563744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568450-C-T

128563947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568306-C-G

128563947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32568306-C-T

128564576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567761-A-G

128564582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567755-G-A

http://identifiers.org/hco/11/GRCh38#128564754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32567580-C-A

128564800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567531-T-A

128564949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32567402-G-A

128565306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32566761-G-T

128565391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32566679-G-A

128565391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32566679-G-T

http://identifiers.org/hco/11/GRCh38#128565402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32566667-A-C

128565458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32566614-T-C

http://identifiers.org/hco/11/GRCh38#128565830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32566075-A-C

128565952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32565956-A-G

128566042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32565866-A-G

128566351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32565558-T-C

128567354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32563306-T-G

128567359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32563301-G-A

128567365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32563294-C-T

128567988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32562517-C-G

128568073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32562440-T-G

128568251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32562247-G-A

128568359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32562112-G-A

128568407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32562064-C-T

128568432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32562046-C-T

128568441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32562037-A-G

128568530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32561950-A-G

128568781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32561700-T-C

128568790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32561691-T-A

128568825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32561655-T-A

128568829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32561651-G-A

http://identifiers.org/hco/11/GRCh38#128568930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32561575-C-A

128572917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560831-A-G

128572917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560831-A-T

128572924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560824-A-G

128572989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560802-A-G

http://identifiers.org/hco/11/GRCh38#128573004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32560787-C-A

128573004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560787-C-T

128573027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560772-G-A

128573027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560772-G-T

128573049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560745-G-A

128573049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560745-G-T

128573087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32560707-T-A

http://identifiers.org/hco/11/GRCh38#128573104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32560690-C-A

128573104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32560690-C-T

http://identifiers.org/hco/11/GRCh38#128573105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32560689-C-A

128573105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32560689-C-G

http://identifiers.org/hco/11/GRCh38#128573109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32560685-C-A

128573146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 32560648-T-C

128573146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 32560648-T-G

128573161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560633-G-A

128573161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560633-G-C

128573161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560633-G-T

128573163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560631-T-A

128573163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560631-T-C

http://identifiers.org/hco/11/GRCh38#128573185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32560609-C-A

128573192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560602-G-A

128573192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560602-G-T

128573236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560559-G-A

128573236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560559-G-T

128573257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560538-T-A

128573257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560538-T-C

http://identifiers.org/hco/11/GRCh38#128573269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32560526-C-A

128573269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560526-C-T

128573314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560482-C-T

128573323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560473-C-T

128573381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560431-A-G

http://identifiers.org/hco/11/GRCh38#128573483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32560323-C-A

128573483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560323-C-G

128573483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560323-C-T

128573535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560255-G-A

128573734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560056-T-C

128573747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32560043-T-G

http://identifiers.org/hco/11/GRCh38#128574204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32559629-C-A

128574228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32559616-G-A

128574538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32559457-C-T

128574617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32559388-C-G

128574625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32559380-A-G

128574651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32559354-C-T

128574652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32559353-G-A

128574861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32559155-T-A

128574915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32559101-T-C

128575063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32558968-C-T

128576458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557945-T-C

128576498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557913-T-C

128576545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557866-T-A

128576555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557856-G-A

128576555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557856-G-T

128576712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557706-C-T

128576893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557555-T-C

128576944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557506-G-A

128577032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557411-C-T

128577044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557399-C-G

128577073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557370-C-T

128577182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557292-T-C

128577293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557185-A-G

128577303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557175-G-C

128577326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557148-A-G

http://identifiers.org/hco/11/GRCh38#128577370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32557114-C-A

128577385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557099-A-T

128577424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32557081-G-A

128577712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32556810-T-C

128578026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32556713-C-G

128578026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32556713-C-T

http://identifiers.org/hco/11/GRCh38#128578141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32556602-C-A

128580047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32555251-T-C

http://identifiers.org/hco/11/GRCh38#128580173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32555169-C-A

128580173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32555169-C-G

128580328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32555056-T-C

http://identifiers.org/hco/11/GRCh38#128580438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32554952-C-A

128580570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32554661-C-G

128580624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32554613-G-T

128580722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32554517-G-A

128580901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32554341-C-G

128580991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32554229-T-C

128581041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32554164-G-A

128581108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32553893-T-G

128581427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32553635-T-A

128581650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32553435-T-C

128581706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32553380-A-G

128581708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32553378-G-T

128581738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32553347-T-A

128581791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32553300-A-G

128582218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32552908-A-G

128582588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32552412-A-T

128582602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32552398-A-T

128582633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32552368-C-T

128582677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32552325-C-T

128582806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32552188-G-C

http://identifiers.org/hco/11/GRCh38#128582818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32552176-A-C

128583169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32551612-T-G

128583177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32551604-C-T

128583305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32551473-C-T

http://identifiers.org/hco/11/GRCh38#128583543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32551162-A-C

http://identifiers.org/hco/11/GRCh38#128583678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32550981-A-C

128584548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32550068-C-T

128584669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32549966-T-G

128585388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32549760-A-G

128585616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32549372-T-A

128585701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32549287-G-C

128585741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32549247-G-A

128585789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32549206-C-T

128586140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32548877-A-G

128586191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32548826-G-A

128586202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32548815-T-G

128586265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32548755-C-T

128586382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32548647-C-G

128586395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32548638-T-G

128586399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32548634-C-G

128586402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32548631-C-T

128587019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32548054-C-G

128587157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32547915-G-T

128587280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32547818-C-T

128587417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32547679-T-A

128587435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32547666-A-G

http://identifiers.org/hco/11/GRCh38#128587485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3488
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32547620-C-A