73073390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85311956-A-G

73073539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85312104-A-G

73073644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85312221-T-C

73073699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85312268-A-G

73073730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85312296-C-T

73073981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85312522-T-C

http://identifiers.org/hco/2/GRCh38#73074009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85312555-C-A

73074051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85312588-T-C

73074053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85312590-C-T

73074141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85312676-A-G

http://identifiers.org/hco/2/GRCh38#73074262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85312796-C-A

73074287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85312821-G-A

73074287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85312821-G-T

73074321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85312855-G-T

http://identifiers.org/hco/2/GRCh38#73074324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85312858-A-C

73074424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85312950-T-C

73074534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85313062-T-G

http://identifiers.org/hco/2/GRCh38#73074563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85313090-C-A

73074563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85313090-C-T

73074569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85313096-G-A

73074569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85313096-G-T

73074630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85313156-T-C

73074630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85313156-T-G

73074641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85313167-A-G

73074691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85313217-G-C

73074691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85313217-G-T

73074730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85313254-G-T

http://identifiers.org/hco/2/GRCh38#73074818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85313341-A-C

http://identifiers.org/hco/2/GRCh38#73074995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85313512-A-C

73074995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85313512-A-T

73075064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85313594-A-G

http://identifiers.org/hco/2/GRCh38#73075089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85313618-A-C

73075392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85313888-G-A

http://identifiers.org/hco/2/GRCh38#73075534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85314018-C-A

73075534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85314018-C-G

73075534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85314018-C-T

73075560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85314044-T-C

73075560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85314044-T-G

73075653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85314137-C-T

73075761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85314246-T-A

73075761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85314246-T-C

73075827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85314285-C-G

73075865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85314335-G-T

http://identifiers.org/hco/2/GRCh38#73076149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85314619-A-C

73076149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85314619-A-G

73076149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85314619-A-T

73076243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85314707-G-A

73076243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85314707-G-T

73076542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85314837-T-C

73076794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85315017-C-T

73076950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85315140-C-T

73077206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85315305-A-G

73077304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85315336-C-T

73077355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85315364-T-C

73077626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85315570-G-A

73079009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85316740-G-A

73079470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85317152-A-G

73079492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85317173-T-C

73079513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85317194-C-G

73079513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85317194-C-T

http://identifiers.org/hco/2/GRCh38#73079517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85317197-C-A

73079517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85317197-C-T

73079564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85317247-G-A

73079564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85317247-G-T

73079604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85317283-T-C

73079725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85317399-T-C

73079725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85317399-T-G

73079787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85317461-C-T

73079818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85317492-A-G

73079854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85317528-A-G

73079854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85317528-A-T

http://identifiers.org/hco/2/GRCh38#73079879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85317553-C-A

73079879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85317553-C-T

73080003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85317677-G-A

73080039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85317713-G-A

73080039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85317713-G-T

http://identifiers.org/hco/2/GRCh38#73080067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85317789-C-A

73080067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85317789-C-G

73080067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85317789-C-T

http://identifiers.org/hco/2/GRCh38#73080072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85317794-C-A

73080096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85317818-A-G

http://identifiers.org/hco/2/GRCh38#73080106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85317828-C-A

73080106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85317828-C-T

73080184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85317897-C-T

73080206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85317919-T-C

73080218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85317931-G-A

73080218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85317931-G-T

73080231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85317944-G-T

73080282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85317995-G-A

73080282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85317995-G-T

http://identifiers.org/hco/2/GRCh38#73080288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85318001-C-A

73080288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85318001-C-T

73080403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85318116-A-G

73080404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85318117-A-G

73080417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85318127-G-A

73080417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85318127-G-T

http://identifiers.org/hco/2/GRCh38#73080462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85318172-C-A

73080462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85318172-C-T

73080474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 85318184-T-A

73080474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85318184-T-C

73080493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85318218-G-A

73080493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85318218-G-C

73080493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85318218-G-T

73080540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85318265-T-C

73080573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85318298-G-T

73080607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85318329-G-A

73080642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85318364-G-A

73080642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85318364-G-C

73080656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85318378-G-A

73080656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85318378-G-T

http://identifiers.org/hco/2/GRCh38#73080664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85318389-A-C

73080664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85318389-A-G

http://identifiers.org/hco/2/GRCh38#73080817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85318542-C-A

73080817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85318542-C-T

73080820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85318545-T-C

73080892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85318617-A-G

73080989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85318714-G-A

73080989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 85318714-G-T

73081462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85319160-A-G

73081462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 85319160-A-T

http://identifiers.org/hco/2/GRCh38#73081503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85319195-C-A

73081503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85319195-C-T

http://identifiers.org/hco/2/GRCh38#73081527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85319219-C-A

73081527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 85319219-C-T

73083509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85320883-A-T

73083958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85321355-T-C

73083972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85321385-G-A

73083980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85321393-T-C

73084102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85321507-A-G

73084190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85321595-C-T

73084214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85321617-C-T

http://identifiers.org/hco/2/GRCh38#73084280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85321670-C-A

73084329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85321736-C-T

73084396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85321858-A-G

73084415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85322085-A-G

73084482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85322149-A-T

73084577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85322241-G-A

http://identifiers.org/hco/2/GRCh38#73085320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85323019-C-A

73085614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85323250-C-T

73086109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85323656-T-C

73086240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85323746-C-G

73086240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85323746-C-T

73086251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85323753-G-T

http://identifiers.org/hco/2/GRCh38#73087002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85323895-C-A

73087331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85324150-C-G

73087729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85324478-G-T

73087969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85324680-T-C

http://identifiers.org/hco/2/GRCh38#73087976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85324687-C-A

73087983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85324694-A-G

73087983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85324694-A-T

http://identifiers.org/hco/2/GRCh38#73088294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85324994-C-A

73088294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 85324994-C-G

73088463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85325151-G-A

http://identifiers.org/hco/2/GRCh38#73088662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85325350-C-A

73088662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 85325350-C-T

73088666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 85325354-G-A

http://identifiers.org/hco/2/GRCh38#73088937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85325595-A-C

73089102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85325760-G-A

73089335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85325990-G-A

http://identifiers.org/hco/2/GRCh38#73089376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85326035-C-A

73089376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85326035-C-T

73089421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85326067-G-A

73089421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85326067-G-T

73089427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85326073-C-T

73089445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85326083-G-A

73089445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85326083-G-T

73089530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85326166-C-T

http://identifiers.org/hco/2/GRCh38#73089544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85326180-C-A

http://identifiers.org/hco/2/GRCh38#73089577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85326212-C-A

73089705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85326330-A-T

http://identifiers.org/hco/2/GRCh38#73089906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#85326428-C-A

http://identifiers.org/hco/2/GRCh38#73090539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85327057-C-A

73090539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85327057-C-T

73090544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85327062-A-G

73090685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85327179-C-T

73090709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85327203-T-C

73091076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85332771-G-A

73091084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85332779-G-A

73091149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85332838-T-C

73091195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85332879-C-T

73091243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85332928-G-A

73091472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85333135-C-T

73091828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85333361-G-C

73091978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85333449-G-A

http://identifiers.org/hco/2/GRCh38#73092244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85333685-C-A

73092722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85334052-G-A

73092982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85334649-C-T

http://identifiers.org/hco/2/GRCh38#73094479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85335266-C-A

73094517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85335304-A-G

73094640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85335424-C-T

73094646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85335427-G-A

http://identifiers.org/hco/2/GRCh38#73094694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85335480-C-A

73097879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85337979-T-C

73097879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85337979-T-G

http://identifiers.org/hco/2/GRCh38#73099410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85338540-A-C

73099675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85338783-G-A

73099765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85338856-T-G

73102850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85343132-C-T

73103009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85343308-G-A

http://identifiers.org/hco/2/GRCh38#73103621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85343929-A-C

73103777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85344086-G-A

http://identifiers.org/hco/2/GRCh38#73103826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85344134-C-A

73103826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85344134-C-T

73103846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85344154-G-A

73103916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85344215-C-T

73104979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85344848-A-G

73105103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85344974-T-C

73105103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85344974-T-G

73106369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85345524-C-T

73106706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85345835-G-A

73106706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85345835-G-T

73106720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85345849-C-T

http://identifiers.org/hco/2/GRCh38#73106811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85345931-C-A

73106990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85346083-G-T

73107255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85346239-A-G

73107551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85346570-G-T

73107577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85346602-G-A

73107577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85346602-G-C

73107712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85346720-G-A

73107977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85346918-C-G

73108473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85347402-G-A

73108483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85347412-A-G

73108577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85347496-A-G

73108578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85347497-T-C

http://identifiers.org/hco/2/GRCh38#73108675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85347594-C-A

73108675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85347594-C-T

73109610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85348257-G-A

73109751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85348371-G-A

73110100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85348741-C-T

73110469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85349054-C-T

http://identifiers.org/hco/2/GRCh38#73110505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85349090-A-C

73110645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85349235-G-A

73110865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85349447-G-A

73111484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85350028-G-A

73111504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85350047-A-T

73111812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85350611-T-A

73112274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85351001-G-A

73112274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85351001-G-T

73112718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 85351451-G-A

73112718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 85351451-G-T

http://identifiers.org/hco/2/GRCh38#73112721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#85351454-C-A

73112721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 85351454-C-T

http://identifiers.org/hco/2/GRCh38#73112945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85351657-C-A

73112945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85351657-C-T

73112948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85351660-T-G

73113128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85351801-C-T

73114965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85354343-G-T

73114998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85354376-A-G

http://identifiers.org/hco/2/GRCh38#73115019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85354394-C-A

73115019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85354394-C-T

73115030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85354405-G-A

73115030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85354405-G-T

73115564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85354696-C-T

73115753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85354807-A-G

73115983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85354958-A-G

73116627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85355760-G-C

73133903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85358233-G-A

73134021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85358346-T-A

73134021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85358346-T-C

73134056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85358377-T-C

73134056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85358377-T-G

73134143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85358749-T-G

73134215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85358809-C-T

73134732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85360094-C-T

http://identifiers.org/hco/2/GRCh38#73134818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#85360177-A-C