http://identifiers.org/hco/16/GRCh38#2988334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23939500-C-A

2988344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 23939490-G-A

2988344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 23939490-G-T

2988396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23939391-T-A

2988396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23939391-T-C

2988396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23939391-T-G

2988553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23939119-T-A

2988565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23939108-A-G

2988580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23939091-G-A

2988580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23939091-G-T

2988625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23939046-A-G

http://identifiers.org/hco/16/GRCh38#2988632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23939040-C-A

2988632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23939040-C-T

http://identifiers.org/hco/16/GRCh38#2988725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23938953-C-A

2988725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23938953-C-T

2988728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23938950-A-G

2988728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23938950-A-T

2988747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23938938-G-A

2988747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23938938-G-C

2988747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23938938-G-T

http://identifiers.org/hco/16/GRCh38#2988846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23938853-C-A

2988846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23938853-C-G

2988846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23938853-C-T

http://identifiers.org/hco/16/GRCh38#2988892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23938815-C-A

2988892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23938815-C-G

2988892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23938815-C-T

2988941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23938763-G-A

2988941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23938763-G-T

2988975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23938740-G-T

2989025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 23938680-G-A

2989025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 23938680-G-T

2989035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23938670-G-T

2989053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23938655-T-A

2989053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23938655-T-C

2989053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23938655-T-G

2989083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938645-G-A

2989083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938645-G-C

2989083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938645-G-T

2989087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938641-G-A

2989087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938641-G-T

2989153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938605-G-C

2989153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938605-G-T

2989225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938522-T-A

2989225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938522-T-C

2989262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938490-T-C

http://identifiers.org/hco/16/GRCh38#2989290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23938462-C-A

2989290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938462-C-T

2989346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938336-G-T

2989393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938054-A-G

2989393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938054-A-T

2989431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938014-G-A

2989431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938014-G-T

2989432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938013-G-A

2989432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23938013-G-T

2989499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23937948-C-T

http://identifiers.org/hco/16/GRCh38#2989517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23937930-C-A

2989517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23937930-C-T

http://identifiers.org/hco/16/GRCh38#2989601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23937856-C-A

2989601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937856-C-G

2989601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937856-C-T

2989615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937822-G-A

2989615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937822-G-T

http://identifiers.org/hco/16/GRCh38#2989623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23937815-C-A

2989623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937815-C-G

2989623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937815-C-T

http://identifiers.org/hco/16/GRCh38#2989667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23937786-C-A

2989668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937785-T-C

2989992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23937396-A-G

2990009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937379-G-A

2990009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937379-G-T

http://identifiers.org/hco/16/GRCh38#2990023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23937368-C-A

2990023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937368-C-G

2990023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937368-C-T

http://identifiers.org/hco/16/GRCh38#2990040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23937351-C-A

2990040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937351-C-T

http://identifiers.org/hco/16/GRCh38#2990059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23937332-C-A

2990059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23937332-C-T

2990103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23937294-T-C

http://identifiers.org/hco/16/GRCh38#2990107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23937290-C-A

2990107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23937290-C-T

2990112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23937285-A-G

2990269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23937165-T-C

http://identifiers.org/hco/16/GRCh38#2990271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23937163-C-A

2990271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23937163-C-T

2990273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23937160-C-G

2990273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23937160-C-T

http://identifiers.org/hco/16/GRCh38#2990534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23936882-C-A

2990534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23936882-C-T

http://identifiers.org/hco/16/GRCh38#2990581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23936835-C-A

2990581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 23936835-C-T

2990632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23936730-T-C

2990633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23936729-G-A

2990633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23936729-G-T

http://identifiers.org/hco/16/GRCh38#2990669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23936683-C-A

2990669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23936683-C-T

http://identifiers.org/hco/16/GRCh38#2990714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23936648-C-A

2990714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23936648-C-T

2990915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23936294-G-A

http://identifiers.org/hco/16/GRCh38#2990947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23936262-C-A

2990947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23936262-C-T

http://identifiers.org/hco/16/GRCh38#2991036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23936199-C-A

http://identifiers.org/hco/16/GRCh38#2991062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23936173-C-A

2991062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23936173-C-T

2991064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23936171-G-A

2991077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23936158-T-A

2991077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23936158-T-C

http://identifiers.org/hco/16/GRCh38#2991123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23936110-C-A

2991123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23936110-C-G

2991123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23936110-C-T

2991229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23936066-T-A

2991229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23936066-T-C

2991239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23936055-G-T

2991329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23935960-T-A

2991329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23935960-T-C

2991383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23935922-G-A

2991383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23935922-G-T

2991385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 23935920-G-A

2991398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23935907-T-A

http://identifiers.org/hco/16/GRCh38#2991433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23935872-A-C

2991433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 23935872-A-G

2991560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23935739-C-G

2991560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23935739-C-T

http://identifiers.org/hco/16/GRCh38#2991872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23935234-C-A

http://identifiers.org/hco/16/GRCh38#2991874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23935232-A-C

2991874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23935232-A-G

http://identifiers.org/hco/16/GRCh38#2991875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23935231-C-A

2991875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23935231-C-T

2991889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23935217-G-T

2991906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23935069-T-C

2991910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23935065-G-A

http://identifiers.org/hco/16/GRCh38#2991994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23934898-C-A

2991994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23934898-C-T

2991996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 23934896-G-A

2991996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 23934896-G-T

2992235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23934659-G-T

2992262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23934633-G-T

http://identifiers.org/hco/16/GRCh38#2992303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23930770-C-A

2992303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930770-C-G

2992303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930770-C-T

2992399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23930655-C-T

2992524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930796-G-A

2992524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930796-G-T

2992544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930770-C-G

2992560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930745-T-C

2992569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930736-A-G

http://identifiers.org/hco/16/GRCh38#2992628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23930655-C-A

2992628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930655-C-T

http://identifiers.org/hco/16/GRCh38#2992682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23930550-C-A

2992682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930550-C-T

http://identifiers.org/hco/16/GRCh38#2992686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23930546-C-A

2992693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930539-G-A

2992693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930539-G-C

2992693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930539-G-T

2992696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930536-A-G

2992710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930513-G-T

http://identifiers.org/hco/16/GRCh38#2992771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23930476-C-A

2992772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23930475-A-G

http://identifiers.org/hco/16/GRCh38#2992791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23932824-C-A

2992791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23932824-C-T

2992822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23932793-G-T

2992902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23932696-G-A

http://identifiers.org/hco/16/GRCh38#2993130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23932493-A-C

2993130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23932493-A-G

2993218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23932446-G-T

http://identifiers.org/hco/16/GRCh38#2993237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23932438-A-C

2993237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23932438-A-G

2994652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931668-G-T

http://identifiers.org/hco/16/GRCh38#2994702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23931601-C-A

2994702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 23931601-C-T

http://identifiers.org/hco/16/GRCh38#2994703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23931600-A-C

2994703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 23931600-A-G

2994704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 23931599-C-T

http://identifiers.org/hco/16/GRCh38#2994709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23931594-C-A

2994709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, stop_gained
orthologous variants: 23931594-C-T

2994718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 23931585-T-C

2994726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, splice_region_variant, synonymous_variant
orthologous variants: 23931577-A-T

2994733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931570-G-C

2994753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931549-A-G

2994762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931540-G-T

http://identifiers.org/hco/16/GRCh38#2994846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23931460-C-A

http://identifiers.org/hco/16/GRCh38#2994868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23931438-C-A

2994868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931438-C-G

2994868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931438-C-T

http://identifiers.org/hco/16/GRCh38#2994913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23931397-A-C

2994913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931397-A-G

http://identifiers.org/hco/16/GRCh38#2994975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23931329-C-A

2994975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931329-C-T

2994992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931315-G-A

2994992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931315-G-C

2994992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931315-G-T

2995061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931237-T-C

2995074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931224-T-C

http://identifiers.org/hco/16/GRCh38#2995151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23931153-C-A

2995151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931153-C-G

2995174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931130-G-A

2995204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931100-G-A

http://identifiers.org/hco/16/GRCh38#2995224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23931076-C-A

2995265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23931051-G-A

2995292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 23931023-G-T

2995414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant
orthologous variants: 23930639-G-T

2995469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23930586-T-C

http://identifiers.org/hco/16/GRCh38#2995488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23930568-C-A

http://identifiers.org/hco/16/GRCh38#2995495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23930561-C-A

2995495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23930561-C-T

2995519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23930550-G-A

2995519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23930550-G-T

http://identifiers.org/hco/16/GRCh38#2995523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23930546-A-C

2995523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23930546-A-G

2995533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23930536-G-T

2995564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23930494-T-C

http://identifiers.org/hco/16/GRCh38#2995582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23930476-A-C

2995582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23930476-A-T

http://identifiers.org/hco/16/GRCh38#2995602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23930462-C-A

2995647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 23930423-T-C

2995650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 23930420-A-G

2995801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23930246-C-G

2995801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23930246-C-T

2995844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23930171-C-T

http://identifiers.org/hco/16/GRCh38#2995854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23930158-C-A

2995854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 23930158-C-T

2995857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 23930155-G-A

2995857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 23930155-G-C

2995857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 23930155-G-T

2995863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant
orthologous variants: 23930147-G-A

2995863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant
orthologous variants: 23930147-G-C

2995863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant
orthologous variants: 23930147-G-T

2996349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929642-T-C

2996407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929582-C-T

http://identifiers.org/hco/16/GRCh38#2996416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23929545-C-A

2996416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929545-C-T

2996555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929421-G-A

2996555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929421-G-T

2996563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929413-T-C

2996594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929381-G-A

2996594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929381-G-T

2996786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929226-G-A

2996786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929226-G-T

2996793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929219-G-A

http://identifiers.org/hco/16/GRCh38#2996801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23929211-C-A

2996801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929211-C-T

2996810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929202-T-G

2996882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929124-T-C

http://identifiers.org/hco/16/GRCh38#2996910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23929095-C-A

2996910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23929095-C-T

2996965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant
orthologous variants: 23929068-T-C

2997064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: missense variant
orthologous variants: 23928959-G-A

2997064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: missense variant
orthologous variants: 23928959-G-T

2997076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: stop gained
orthologous variants: 23928947-C-T

2997095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928928-G-A

2997095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928928-G-C

2997095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928928-G-T

http://identifiers.org/hco/16/GRCh38#2997195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23928816-C-A

2997195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928816-C-T

2997220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928786-T-C

2997295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928740-G-A

2997295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928740-G-C

2997331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928696-C-G

2997331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928696-C-T

2997406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant
orthologous variants: 23928650-G-A

2997406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant
orthologous variants: 23928650-G-T

2997468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928581-G-A

2997468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928581-G-C

2997468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928581-G-T

2997543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928514-G-A

2997543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928514-G-T

http://identifiers.org/hco/16/GRCh38#2997556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23928501-C-A

2997556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23928501-C-T

2997811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: missense variant
orthologous variants: 23934898-G-A

2997813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: synonymous variant
orthologous variants: 23934896-G-A

2997813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: missense variant
orthologous variants: 23934896-G-C

2997813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: missense variant
orthologous variants: 23934896-G-T

2998047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927937-T-G

2998131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927857-C-T

2998207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927769-T-C

2998241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 23927735-G-A

2998316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927624-G-A

2998334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927609-G-A

2998334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927609-G-T

http://identifiers.org/hco/16/GRCh38#2998368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23927576-C-A

2998368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: missense variant
orthologous variants: 23927576-C-G

2998368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: missense variant
orthologous variants: 23927576-C-T

2998519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, stop_gained
orthologous variants: 23927483-G-A

2998555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927446-A-G

2998560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927441-G-A

2998560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927441-G-T

2998592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927413-G-A

2998592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927413-G-C

2998685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927345-G-A

http://identifiers.org/hco/16/GRCh38#2998746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23927299-C-A

2998746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927299-C-T

2998810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927237-G-A

http://identifiers.org/hco/16/GRCh38#2998867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23927182-C-A

2998867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: synonymous variant
orthologous variants: 23927182-C-T

2998999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927047-G-A

2998999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23927047-G-T

http://identifiers.org/hco/16/GRCh38#2999067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23926996-C-A

2999246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23926930-T-C

2999250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 23926926-T-C

http://identifiers.org/hco/16/GRCh38#2999264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23926912-C-A

2999264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant
orthologous variants: 23926912-C-T

2999379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23926808-A-G

2999386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23926801-G-T

http://identifiers.org/hco/16/GRCh38#2999400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23926792-C-A

2999400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23926792-C-G

2999803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23926675-G-A

http://identifiers.org/hco/16/GRCh38#2999827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23926651-C-A

http://identifiers.org/hco/16/GRCh38#2999834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23926644-C-A

2999834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23926644-C-T

2999867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23926618-T-C

2999867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23926618-T-G

http://identifiers.org/hco/16/GRCh38#2999935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23926545-C-A

2999935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: missense variant
orthologous variants: 23926545-C-T

2999979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23926507-T-C

http://identifiers.org/hco/16/GRCh38#3000001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23926490-C-A

3000001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23926490-C-T

http://identifiers.org/hco/16/GRCh38#3000013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23926478-C-A

3000017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23926474-G-A

3000036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23926455-T-C

3000298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant
orthologous variants: 23925292-G-A

3000377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23925201-G-A

3000377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23925201-G-T

http://identifiers.org/hco/16/GRCh38#3000476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23925110-A-C

3000557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 23925026-A-G

3000603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 23924980-T-A

3000603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 23924980-T-G

http://identifiers.org/hco/16/GRCh38#3000642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23924943-C-A

3000642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 23924943-C-T

3000656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 23924915-G-A

3000656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 23924915-G-C

3000692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 23924863-C-T

http://identifiers.org/hco/16/GRCh38#3000701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23924854-C-A

3000701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 23924854-C-G

3000842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924749-G-A

3000842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924749-G-T

3000848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924743-G-T

3000909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924698-A-G

3000923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924678-A-G

3000926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924675-A-G

3000984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924635-G-A

3001074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924594-G-A

3001093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924575-A-G

3001102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924566-A-G

3001133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924552-T-C

3001159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924525-A-G

3001159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924525-A-T

3001217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924469-A-G

3001271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924414-T-C

3001271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924414-T-G

3001458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924266-G-A

3001458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924266-G-T

3001538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924230-A-G

3001538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron variant
orthologous variants: 23924230-A-T

http://identifiers.org/hco/16/GRCh38#3001553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23924215-C-A

3001703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3 prime UTR variant
orthologous variants: 23924024-G-A

3001703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3 prime UTR variant
orthologous variants: 23924024-G-T

http://identifiers.org/hco/16/GRCh38#3001708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23924019-C-A

3001708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3 prime UTR variant
orthologous variants: 23924019-C-T

3001709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3 prime UTR variant
orthologous variants: 23924018-G-A

3001722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3 prime UTR variant
orthologous variants: 23924005-G-A

3001722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3 prime UTR variant
orthologous variants: 23924005-G-C

3001722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3 prime UTR variant
orthologous variants: 23924005-G-T

http://identifiers.org/hco/16/GRCh38#3001802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#23923944-A-C

3001802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3 prime UTR variant
orthologous variants: 23923944-A-G

3001886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3 prime UTR variant
orthologous variants: 23923872-G-A

3001912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3 prime UTR variant
orthologous variants: 23923846-G-A

3001912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27549
most severe consequence: 3 prime UTR variant
orthologous variants: 23923846-G-T