20228657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35090398-G-A

http://identifiers.org/hco/15/GRCh38#20228684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35090371-C-A

20228684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35090371-C-T

20228720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35090335-G-A

20228720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35090335-G-C

20228741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35090314-T-A

20228741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35090314-T-C

http://identifiers.org/hco/15/GRCh38#20228977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35090092-C-A

20228977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35090092-C-G

20228977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35090092-C-T

20229025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35090053-G-C

20229025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35090053-G-T

20232178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35088240-C-T

20237957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35085523-C-G

20237987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35085492-T-C

20237996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35085483-G-A

20239243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35085062-G-A

20239298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084995-A-G

http://identifiers.org/hco/15/GRCh38#20239301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35084992-C-A

20239301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084992-C-G

20239301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084992-C-T

20239312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084981-C-G

20239312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084981-C-T

20239314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084979-G-A

20239314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084979-G-C

20239316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084977-G-A

20239316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084977-G-T

20239319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084974-T-A

20239320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084973-C-T

20239378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084924-G-A

20239378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084924-G-C

20239378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084924-G-T

20239394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35084913-G-A

20239394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35084913-G-C

20239394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35084913-G-T

http://identifiers.org/hco/15/GRCh38#20239481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35084826-A-C

20239508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35084799-T-A

http://identifiers.org/hco/15/GRCh38#20239563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35084744-A-C

20239563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35084744-A-T

http://identifiers.org/hco/15/GRCh38#20239641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35084662-C-A

20239641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084662-C-T

20239643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084660-T-A

20239643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084660-T-C

20240611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084288-A-G

20240630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084269-A-G

20240630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084269-A-T

20240654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084232-G-A

20240661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084225-G-A

20240661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084225-G-T

http://identifiers.org/hco/15/GRCh38#20240745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35084158-C-A

20240745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35084158-C-T

20240772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35084131-T-C

20240772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35084131-T-G

20240853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084050-G-A

20240853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084050-G-C

20240853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084050-G-T

20240860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084043-G-A

20240860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084043-G-C

20240860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084043-G-T

20240872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084032-A-G

20240879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35084025-G-A

http://identifiers.org/hco/15/GRCh38#20240893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35083988-C-A

20240893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35083988-C-G

20240893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35083988-C-T

20240919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35083959-G-A

20240919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35083959-G-C

20240919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35083959-G-T

20240958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35083931-A-G

20241007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35083886-G-A

20241055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35083838-T-C

20241078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35083816-T-C

20241078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35083816-T-G

20242825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35083501-T-G

20242848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35083478-T-C

20242859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 35083467-A-G

http://identifiers.org/hco/15/GRCh38#20242920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35083406-C-A

20242979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35083350-T-C

20244773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35081099-T-C

http://identifiers.org/hco/15/GRCh38#20244783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35081089-C-A

20244783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35081089-C-T

20244825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35081044-G-A

20244825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35081044-G-C

http://identifiers.org/hco/15/GRCh38#20244873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35080983-C-A

20244873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35080983-C-G

20244873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35080983-C-T

20244882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35080979-G-A

20244882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35080979-G-C

20244882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35080979-G-T

20244918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35080940-G-A

20244918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35080940-G-C

20244918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35080940-G-T

20244939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35080919-T-C

20244939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35080919-T-G

http://identifiers.org/hco/15/GRCh38#20245023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35080835-C-A

20245023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35080835-C-T

20248596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35079204-T-A

20248787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35078985-G-A

20248787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35078985-G-T

20248796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35078976-A-T

20248798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35078974-C-G

20248798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35078974-C-T

20248815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35078956-C-G

20248815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35078956-C-T

20248816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35078955-T-C

20248846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35078930-A-G

http://identifiers.org/hco/15/GRCh38#20251236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35076682-C-A

20251236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076682-C-G

20251236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076682-C-T

http://identifiers.org/hco/15/GRCh38#20251240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35076678-C-A

20251240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076678-C-G

20251240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076678-C-T

20251273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076644-T-A

20251273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076644-T-C

http://identifiers.org/hco/15/GRCh38#20251277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35076640-C-A

20251277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076640-C-T

20251316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076601-A-G

http://identifiers.org/hco/15/GRCh38#20251320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35076598-C-A

20251320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076598-C-T

20251326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076592-G-A

20251326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076592-G-T

20251397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35076533-A-G

http://identifiers.org/hco/15/GRCh38#20251401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35076529-C-A

20251401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35076529-C-T

20251466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35076464-T-C

http://identifiers.org/hco/15/GRCh38#20251566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35076365-C-A

20251566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076365-C-G

20251566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076365-C-T

http://identifiers.org/hco/15/GRCh38#20251638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35076297-C-A

20251638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076297-C-T

http://identifiers.org/hco/15/GRCh38#20251656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35076279-C-A

20251656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076279-C-G

20251656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076279-C-T

20251758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076178-A-T

20251822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076114-G-A

20251822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076114-G-T

20251823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076113-G-A

20251823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076113-G-T

20251827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076109-T-C

http://identifiers.org/hco/15/GRCh38#20251844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35076092-C-A

20251844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076092-C-T

20251862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076074-G-C

20251862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076074-G-T

20251881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076027-A-G

20251881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076027-A-T

20251882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076026-G-A

http://identifiers.org/hco/15/GRCh38#20251887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35076021-C-A

20251887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076021-C-G

20251887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35076021-C-T

20251950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35075763-G-A

20251950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35075763-G-C

20251983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35075730-T-A

20251983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35075730-T-C

http://identifiers.org/hco/15/GRCh38#20251995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35075718-C-A

20252070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35075643-G-A

20252070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35075643-G-C

20252070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35075643-G-T

20252132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 35075581-T-C

20254671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073801-T-C

20254672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073800-A-G

20254777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073737-G-A

20254777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073737-G-T

20255668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073262-G-A

20255678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073252-G-T

20255704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073229-G-A

20255712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073221-C-G

20255771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073174-G-A

20255771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073174-G-C

20255779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073166-C-G

20255789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073164-G-A

20255790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073163-G-A

20255790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073163-G-C

20255801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073152-C-G

20255801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073152-C-T

20255804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073149-G-C

20255861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073103-G-A

20255861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073103-G-C

20255861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073103-G-T

20255876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073088-G-A

20255876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073088-G-C

20255880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35073084-C-T

20256732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35072276-C-T

20256738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35072270-T-A

20256738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35072270-T-C

20256740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35072268-C-T

20256753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35072253-T-C

20256755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35072251-T-C

20256790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35072216-T-C

20257182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35072007-G-A

20257182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35072007-G-C

20257182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35072007-G-T

20257198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071991-G-A

20257198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071991-G-C

20257198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071991-G-T

http://identifiers.org/hco/15/GRCh38#20257205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35071984-A-C

20257205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071984-A-G

20257205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071984-A-T

http://identifiers.org/hco/15/GRCh38#20257260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35071919-C-A

20257260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071919-C-T

http://identifiers.org/hco/15/GRCh38#20257293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35071886-C-A

20257293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35071886-C-G

20257293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35071886-C-T

20257491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071686-G-A

20257491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071686-G-C

20257491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071686-G-T

20257501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071676-T-C

20257501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071676-T-G

20257745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071423-G-A

20257746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071422-T-C

20257749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071419-T-C

20257760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071408-G-A

20257760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071408-G-T

http://identifiers.org/hco/15/GRCh38#20257785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35071361-C-A

20257785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071361-C-T

http://identifiers.org/hco/15/GRCh38#20261236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35071148-C-A

20261236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071148-C-T

http://identifiers.org/hco/15/GRCh38#20261288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35071105-A-C

20261288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071105-A-G

20261289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071104-T-C

20261322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071072-T-C

http://identifiers.org/hco/15/GRCh38#20261358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35071036-C-A

20261365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071029-G-A

20261371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071023-T-C

20261372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071022-C-G

20261372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35071022-C-T

20261489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070950-G-A

20261527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070897-T-A

20261527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070897-T-G

20261613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070806-G-A

20261613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070806-G-T

20261626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070796-G-A

20261637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070793-C-T

20261694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070731-C-G

20261713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070712-G-A

20261902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35070632-G-C

20261902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35070632-G-T

20262021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070518-G-A

20262021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070518-G-C

20262021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070518-G-T

20262047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070505-C-G

20262047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070505-C-T

http://identifiers.org/hco/15/GRCh38#20262051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35070501-C-A

20262051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070501-C-T

20262136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070439-T-A

20262136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070439-T-C

20262136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070439-T-G

20262145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070430-G-T

20262176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070397-C-T

20262212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070371-C-T

20262222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070361-C-G

20262222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070361-C-T

20262225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070358-T-C

20262701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070330-A-G

20262709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070322-A-G

20262709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070322-A-T

http://identifiers.org/hco/15/GRCh38#20262781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35070256-C-A

20262781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070256-C-T

http://identifiers.org/hco/15/GRCh38#20262807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35070227-C-A

20262807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070227-C-T

http://identifiers.org/hco/15/GRCh38#20262815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35070219-C-A

20262815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070219-C-G

20262815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35070219-C-T

20262861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35070181-T-C

20266931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35065115-G-C

20266945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35065101-C-T

20267057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35064985-G-A

20267057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35064985-G-C

20267164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35064860-T-C

20267194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35064829-A-G

20267194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35064829-A-T

20267216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35064688-G-A

20267219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35064685-G-A

20267221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35064683-A-G

20267224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35064680-G-A

20267274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35064626-T-C

20267279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35064621-G-T

20267283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35064617-A-G

20271287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35063313-G-A

http://identifiers.org/hco/15/GRCh38#20271603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35063181-C-A

20271603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35063181-C-G

20271603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35063181-C-T

20271800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062986-G-A

20271800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062986-G-C

20271800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062986-G-T

http://identifiers.org/hco/15/GRCh38#20271801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35062985-C-A

20271801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062985-C-T

20271817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062975-A-G

20271820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062972-A-G

20271820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062972-A-T

http://identifiers.org/hco/15/GRCh38#20271841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35062960-C-A

20271841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062960-C-T

http://identifiers.org/hco/15/GRCh38#20272857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#35062459-C-A

20272857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35062459-C-T

20272957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35062359-T-A

20273034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35062281-T-C

20273062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062221-T-A

20273062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062221-T-C

http://identifiers.org/hco/15/GRCh38#20273110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35062169-C-A

20273110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062169-C-T

20273117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062163-C-T

20273122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062158-G-T

20273130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062128-C-T

20273273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062038-C-G

20273273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35062038-C-T

20274619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35061702-A-T

20274648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35061672-G-A

20274717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35061599-C-T

http://identifiers.org/hco/15/GRCh38#20274841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35061489-A-C

20274883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35061445-G-A

20274883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35061445-G-T

20274945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35061410-T-C

http://identifiers.org/hco/15/GRCh38#20274968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35061389-C-A

20274968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35061389-C-G

20274973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35061384-T-C

20275018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35061323-C-T

20275020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35061321-C-T

20275109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35061224-A-G

20275113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35061220-T-A

20275117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35061216-C-G

20275117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35061216-C-T

http://identifiers.org/hco/15/GRCh38#20276707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35060556-C-A

20276707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35060556-C-T

20276710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35060553-C-T

20276716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35060547-G-A

20276716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35060547-G-T

http://identifiers.org/hco/15/GRCh38#20276878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35060369-A-C

20276878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060369-A-G

20276878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060369-A-T

20277008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060253-G-A

20277023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060238-G-A

20277023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060238-G-C

20277023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060238-G-T

20277030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060230-T-C

20277030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060230-T-G

20277036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060225-T-A

20277036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060225-T-C

20277079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060182-T-A

20277079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060182-T-C

20277079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060182-T-G

20277101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060152-T-C

http://identifiers.org/hco/15/GRCh38#20277124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#35060129-C-A

20277124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060129-C-G

20277124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37708
most severe consequence: non coding transcript exon variant
orthologous variants: 35060129-C-T