55488482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 5 prime UTR variant
orthologous variants: 4928856-G-A

55488482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 5 prime UTR variant
orthologous variants: 4928856-G-T

55488581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4928945-G-A

55488588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4928952-C-G

55488588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4928952-C-T

55488644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929019-G-T

http://identifiers.org/hco/19/GRCh38#55488659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4929034-C-A

55488659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929034-C-T

55488671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929047-C-G

55488671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929047-C-T

55488691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929067-G-A

55488691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929067-G-T

55488701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929077-T-G

http://identifiers.org/hco/19/GRCh38#55488731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4929114-C-A

55488731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929114-C-T

55488761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929145-A-G

55488917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929400-G-A

55488917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929400-G-T

http://identifiers.org/hco/19/GRCh38#55488962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4929448-C-A

55488962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929448-C-G

55488962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929448-C-T

http://identifiers.org/hco/19/GRCh38#55489040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4929523-C-A

55489040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 4929523-C-T

55489076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4929557-G-A

55489076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4929557-G-C

55489076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4929557-G-T

http://identifiers.org/hco/19/GRCh38#55489077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4929558-C-A

55489077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4929558-C-G

55489077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4929558-C-T

http://identifiers.org/hco/19/GRCh38#55489080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4929561-C-A

55489080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4929561-C-G

55489080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4929561-C-T

http://identifiers.org/hco/19/GRCh38#55489081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4929562-C-A

55489081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4929562-C-G

55489081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4929562-C-T

55489261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4929880-A-G

55489303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4929922-G-A

55489303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4929922-G-T

55489469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4930088-G-A

55489469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4930088-G-T

55489547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4930166-G-A

55489583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4930202-G-A

55489583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4930202-G-T

55489606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4930225-G-A

55489606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4930225-G-T

55489765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930369-G-A

55489765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930369-G-C

http://identifiers.org/hco/19/GRCh38#55489774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4930378-C-A

55489774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930378-C-T

55489777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930381-C-G

55489805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930471-C-G

55489839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930503-C-G

55489847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930511-T-C

55489982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4930651-C-G

http://identifiers.org/hco/19/GRCh38#55490188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4930771-C-A

55490190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930773-T-G

http://identifiers.org/hco/19/GRCh38#55490237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4930830-C-A

55490237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930830-C-T

55490247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930840-G-A

55490247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930840-G-T

55490248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930841-A-G

http://identifiers.org/hco/19/GRCh38#55490265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4930858-C-A

55490265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930858-C-T

http://identifiers.org/hco/19/GRCh38#55490433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4931030-A-C

55490433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4931030-A-G

55490433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4931030-A-T

55490452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4931050-T-A

55490452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4931050-T-C

55490452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4931050-T-G

http://identifiers.org/hco/19/GRCh38#55490524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4931119-A-C

55490524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4931119-A-G

55490524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4931119-A-T

http://identifiers.org/hco/19/GRCh38#55490708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4931287-C-A

55490708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4931287-C-T

http://identifiers.org/hco/19/GRCh38#55490800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4931412-C-A

55490800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4931412-C-T

55490887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4931499-A-G

http://identifiers.org/hco/19/GRCh38#55491025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4931637-C-A

55491025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4931637-C-T

55491067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4931679-G-T

http://identifiers.org/hco/19/GRCh38#55493555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4932195-C-A

55493555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4932195-C-G

55493555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4932195-C-T

55493562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4932202-T-C

http://identifiers.org/hco/19/GRCh38#55493569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4932209-C-A

55493707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4932348-A-G

55493852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4932493-G-A

55493852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4932493-G-C

http://identifiers.org/hco/19/GRCh38#55493893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4932534-C-A

55493893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4932534-C-T

55494053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4932696-T-A

55494055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4932698-T-A

55494055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4932698-T-C

55494444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4932924-G-A

55494611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 4933002-C-T

55494677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4933056-T-C

55494701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4933080-G-A

55494861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4933202-G-A

55494861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4933202-G-C

55494861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4933202-G-T

http://identifiers.org/hco/19/GRCh38#55494866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4933207-C-A

55494866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4933207-C-G

55494866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4933207-C-T

55494884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4933226-G-A

55494904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4933246-G-A

55494953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4933290-G-C

55497720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4935949-C-T

55497823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4936053-A-T

55497929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 4936183-A-G

55497992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 4936246-T-C

55498185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, missense_variant
orthologous variants: 4936439-G-A

55498227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4936481-C-T

http://identifiers.org/hco/19/GRCh38#55498266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4936522-C-A

55498266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4936522-C-T

55498325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4936577-A-G

55498662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4936705-G-A

55498855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4936893-G-C

55498920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4936958-C-T

55499005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4937029-G-A

55499016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4937040-A-G

http://identifiers.org/hco/19/GRCh38#55499091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4937130-C-A

55499091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4937130-C-T

55499092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4937131-G-A

http://identifiers.org/hco/19/GRCh38#55499234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4937278-C-A

55499381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4937407-G-A

55499381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4937407-G-C

55499824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4939270-G-A

55499964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4939407-G-A

http://identifiers.org/hco/19/GRCh38#55499969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4939412-C-A

55499969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4939412-C-T

55500071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4939514-C-T

55500167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4939580-C-T

http://identifiers.org/hco/19/GRCh38#55500213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4939626-C-A

55500364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4939777-C-T

http://identifiers.org/hco/19/GRCh38#55500463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4939875-C-A

55500463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4939875-C-T

55500557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4939974-C-T

http://identifiers.org/hco/19/GRCh38#55500662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4940079-C-A

55500662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4940079-C-G

55500751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4940168-C-T

55500847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4940246-C-T

55500888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4940283-G-T

55500920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4940330-G-A

55501040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4940470-C-G

55501120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4940550-G-A

55501120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4940550-G-T

55501162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4940592-G-C

55501169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4940599-C-T

55501187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4940617-G-A

55501187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4940617-G-T

55501197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4940627-C-T

55501421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4941049-G-T

55501441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4941066-T-C

55501592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4941188-G-A

55503122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4942682-G-A

55503125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4942689-G-A

55503192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4942737-C-T

55503290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4942812-C-T

55503353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4942854-G-A

55503370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4942871-C-T

55503419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4942902-C-T

55503486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4942973-C-T

55503695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4942992-C-T

55503717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, undefined
orthologous variants: 4943014-G-A

55504011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4943213-G-A

55504011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4943213-G-T

55504033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, undefined
orthologous variants: 4943224-G-A

55504041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, undefined
orthologous variants: 4943232-G-A

55504076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, undefined
orthologous variants: 4943245-G-A

55504186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, stop_lost
orthologous variants: 4943378-G-C

55504189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4943381-C-T

55504203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4943395-G-A

55504203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4943395-G-C

55504283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4943466-G-C

55504295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4943468-G-A

http://identifiers.org/hco/19/GRCh38#55504298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#4943471-C-A

55504298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 4943471-C-G

55505012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4944069-T-G

55505085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4944144-A-G

55505124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4944176-G-A

55505192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4944230-G-T

55505251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4944288-G-A

55505269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4944306-C-T

55513032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4945734-T-C

55513064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4945766-G-A

55513067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4945769-C-G

55513067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4945769-C-T

55513084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4945786-T-A

55513084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4945786-T-C

http://identifiers.org/hco/19/GRCh38#55513161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4945866-A-C

55513191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4945883-G-A

55513191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4945883-G-T

http://identifiers.org/hco/19/GRCh38#55513242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4945934-C-A

55513242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4945934-C-G

55513242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: 4945934-C-T

http://identifiers.org/hco/19/GRCh38#55513249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4945941-C-A

http://identifiers.org/hco/19/GRCh38#55513257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4945953-C-A

55517090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, undefined
orthologous variants: 4946410-G-T

http://identifiers.org/hco/19/GRCh38#55517114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#4946434-C-A

55517114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, undefined
orthologous variants: 4946434-C-G

55517114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, undefined
orthologous variants: 4946434-C-T

55517116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, undefined
orthologous variants: 4946436-A-G

55517140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: intron_variant, undefined
orthologous variants: 4946460-G-A

http://identifiers.org/hco/19/GRCh38#55517275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4946598-C-A

55517275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4946598-C-T

55517300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4946611-C-T

http://identifiers.org/hco/19/GRCh38#55517354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4946665-C-A

55517421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4946726-C-T

http://identifiers.org/hco/19/GRCh38#55517514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4946792-C-A

55517514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4946792-C-T

55517567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4946845-G-A

55517598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4946876-G-A

55517612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4946890-C-G

55517612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4946890-C-T

55517644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4946922-C-T

55517690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4946950-A-G

55517695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4946955-C-T

55517702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4946962-C-G

55517702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4946962-C-T

55518082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4946994-T-A

55518082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4946994-T-C

55518082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4946994-T-G

http://identifiers.org/hco/19/GRCh38#55518089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4947001-C-A

55518089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4947001-C-T

http://identifiers.org/hco/19/GRCh38#55518092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4947004-C-A

55518113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4947025-G-A

55518113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4947025-G-C

55518113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4947025-G-T

55518137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4947049-T-A

55518137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4947049-T-C

http://identifiers.org/hco/19/GRCh38#55518151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4947063-C-A

55518151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4947063-C-T

http://identifiers.org/hco/19/GRCh38#55518162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4947074-A-C

55518162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4947074-A-G

55518162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4947074-A-T

http://identifiers.org/hco/19/GRCh38#55518166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4947078-C-A

55518166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4947078-C-T

http://identifiers.org/hco/19/GRCh38#55518187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4947099-C-A

55518187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4947099-C-T

http://identifiers.org/hco/19/GRCh38#55518193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4947105-A-C

55518321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4947200-C-G

55518321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4947200-C-T

http://identifiers.org/hco/19/GRCh38#55518376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4947240-C-A

55518415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4947276-T-C

55518454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4947315-C-T

http://identifiers.org/hco/19/GRCh38#55518705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4947470-A-C

55518705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4947470-A-G

55518758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4947523-G-A

55518804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4947569-G-C

55518848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: synonymous variant
orthologous variants: 4947613-G-A

55518861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4947626-G-A

http://identifiers.org/hco/19/GRCh38#55518885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4947650-C-A

55518897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4947662-G-A

55518904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: 4947669-A-G

http://identifiers.org/hco/19/GRCh38#55518927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4947692-A-C

http://identifiers.org/hco/19/GRCh38#55519084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4947824-C-A

http://identifiers.org/hco/19/GRCh38#55519085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#4947825-A-C

55519085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26641
most severe consequence: 3 prime UTR variant
orthologous variants: 4947825-A-G