http://identifiers.org/hco/3/GRCh38#128909876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87652260-C-A

128909876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87652260-C-T

128909967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87652351-T-C

128909971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 87652355-G-A

128909971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87652355-G-T

128910098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 87652461-G-A

128910271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87652713-G-C

128910271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87652713-G-T

http://identifiers.org/hco/3/GRCh38#128910319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87652864-C-A

128910319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87652864-C-G

http://identifiers.org/hco/3/GRCh38#128910477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87653012-C-A

128910477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 87653012-C-T

128910746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 87653229-C-G

128910746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 87653229-C-T

128910771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 87653254-G-A

128910798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 87653281-T-C

128910830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87653311-G-A

128910846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87653327-G-A

128910846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87653327-G-T

128910910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87653381-G-T

128911794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87653506-T-G

128911840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87653531-C-G

128911898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87653590-T-A

128912060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87653713-C-T

128912121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87653772-A-G

128912341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87653901-T-C

http://identifiers.org/hco/3/GRCh38#128912360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87653907-C-A

128912360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87653907-C-T

128912413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87653962-G-A

128912413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87653962-G-T

128912615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87654139-G-A

128912615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87654139-G-C

128912624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87654148-C-T

128912819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87654811-G-T

128912824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87654816-G-C

128912957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87654905-G-C

128912957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87654905-G-T

128913063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87655008-A-G

128913149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87655096-C-T

128913174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87655113-A-G

128913202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87655138-C-G

128913202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87655138-C-T

128913367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87655313-T-C

128913478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87655402-T-A

128913478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87655402-T-G

128913510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87655434-A-G

128913818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87655641-G-A

128913855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87655680-A-G

128914019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87655801-C-T

128914042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87655824-G-A

128914577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87656297-T-A

128914683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87656380-T-C

128914683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87656380-T-G

128914741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87656450-G-A

128914741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87656450-G-T

http://identifiers.org/hco/3/GRCh38#128914747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87656458-C-A

http://identifiers.org/hco/3/GRCh38#128914823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87656530-C-A

128914937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87656643-T-C

http://identifiers.org/hco/3/GRCh38#128914975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87656671-C-A

128914975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87656671-C-G

128914975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87656671-C-T

128914987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87656683-T-C

128914993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87656688-T-C

128915031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87656726-T-C

http://identifiers.org/hco/3/GRCh38#128915059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87656754-C-A

128915059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87656754-C-T

128915145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 87656835-G-A

128915145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 87656835-G-T

128915147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 87656837-G-A

128915177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 87656867-G-A

128915177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, stop_gained, undefined
orthologous variants: 87656867-G-T

128915234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 87656924-A-G

128915305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 87656995-G-C

http://identifiers.org/hco/3/GRCh38#128915327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87657017-C-A

128915327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 87657017-C-G

128915337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 87657027-C-T

http://identifiers.org/hco/3/GRCh38#128915366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87657056-C-A

128915366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 87657056-C-T

http://identifiers.org/hco/3/GRCh38#128915543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87657233-C-A

128915543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 87657233-C-T

128915579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87657267-G-C

128915579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87657267-G-T

128915592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87657280-G-T

128915596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87657298-G-A

128915596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87657298-G-T

http://identifiers.org/hco/3/GRCh38#128915781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87657461-C-A

128915781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87657461-C-T

http://identifiers.org/hco/3/GRCh38#128915843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87657514-C-A

128915843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87657514-C-T

http://identifiers.org/hco/3/GRCh38#128915911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87657581-C-A

128916092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87657944-G-A

128916092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87657944-G-T

128916095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87658074-T-C

128916095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87658074-T-G

128916221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 87658200-C-T

128916303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87658282-C-T

http://identifiers.org/hco/3/GRCh38#128916390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87658354-C-A

128916390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87658354-C-T

128916652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87658626-G-T

128916669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87658638-G-A

128916741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, undefined
orthologous variants: 87658715-G-C

128932255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87666691-C-T

128932310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87666784-T-C

http://identifiers.org/hco/3/GRCh38#128932557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87667092-C-A

128932557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87667092-C-T

128932560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87667095-G-A

128932560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87667095-G-T

http://identifiers.org/hco/3/GRCh38#128932569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87667104-C-A

128932569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87667104-C-T

http://identifiers.org/hco/3/GRCh38#128932588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87667124-C-A

128932588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87667124-C-T

128932619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87667138-T-G

http://identifiers.org/hco/3/GRCh38#128932623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87667142-C-A

128932623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87667142-C-T

http://identifiers.org/hco/3/GRCh38#128932649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87667167-A-C

http://identifiers.org/hco/3/GRCh38#128932806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87667636-C-A

128932806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant
orthologous variants: 87667636-C-T

128932850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 87667680-G-A

128932973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 87667803-G-A

128932979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 87667809-A-G

http://identifiers.org/hco/3/GRCh38#128933011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87667841-C-A

128933011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87667841-C-G

128933011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87667841-C-T

128933058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87667873-C-T

http://identifiers.org/hco/3/GRCh38#128933113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87667917-C-A

128933113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87667917-C-G

128933115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87667919-T-C

128934917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87671482-T-A

http://identifiers.org/hco/3/GRCh38#128934993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87671556-C-A

128934994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87671557-T-A

128934994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87671557-T-C

128935017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87671615-G-A

128935017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87671615-G-C

128935017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87671615-G-T

128935044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87671652-G-A

128935044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87671652-G-T

128935048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87671656-G-T

http://identifiers.org/hco/3/GRCh38#128935078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87671683-C-A

128935078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87671683-C-T

128935118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 87671701-T-C

128935220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 87671803-G-A

128935220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant
orthologous variants: 87671803-G-T

128935341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87671916-G-A

128935341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87671916-G-T

http://identifiers.org/hco/3/GRCh38#128935363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87671937-C-A

http://identifiers.org/hco/3/GRCh38#128935392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87671969-C-A

128935394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87671971-G-A

128935394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87671971-G-T

http://identifiers.org/hco/3/GRCh38#128944991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87674956-C-A

128944995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87674960-G-T

128945012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87674978-C-T

128945103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 87675069-G-A

128945166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 87675132-A-T

128945430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 87675396-C-T

128945636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87675602-T-C

128945727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87675693-A-T

128945867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87675833-T-C

128945961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87675927-A-G

128945967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 87675933-G-T

http://identifiers.org/hco/3/GRCh38#128945970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87675936-C-A

128945970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87675936-C-T

128946255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87676178-T-C

128946266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87676189-T-G

128946297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87676217-T-C

128946327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87676247-G-A

128946327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87676247-G-T

128965398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87677162-A-T

128965433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87677201-G-T

128965434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87677202-G-T

128965553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 87677323-A-G

128965706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87677477-T-A

128965706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87677477-T-C

http://identifiers.org/hco/3/GRCh38#128965715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87677486-C-A

128965869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron variant
orthologous variants: 87682056-C-T

128967982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87682765-G-A

128968013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87682794-G-A

128968026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87682807-G-T

http://identifiers.org/hco/3/GRCh38#128968069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87682841-A-C

128968069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87682841-A-G

128968069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87682841-A-T

128968087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87682860-A-G

128968087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87682860-A-T

http://identifiers.org/hco/3/GRCh38#128968155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87682932-C-A

128968155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87682932-C-T

128968156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87682933-A-G

128968196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87682971-G-A

http://identifiers.org/hco/3/GRCh38#128968204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87682979-A-C

128968309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87683072-T-C

128968411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87683149-G-A

http://identifiers.org/hco/3/GRCh38#128968449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87683187-C-A

128968449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87683187-C-T

128970391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87683420-T-C

128970428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87683452-C-T

128970510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87683543-G-A

128970515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87683548-A-G

128970661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87683691-T-C

128970661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87683691-T-G

http://identifiers.org/hco/3/GRCh38#128970882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87683908-C-A

128970882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87683908-C-G

128970882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87683908-C-T

128971455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87684398-A-G

128971478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87684417-T-C

http://identifiers.org/hco/3/GRCh38#128971479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87684418-C-A

128971479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87684418-C-T

128971483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87684422-G-A

128971483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87684422-G-C

128971483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87684422-G-T

128971515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87684452-G-T

http://identifiers.org/hco/3/GRCh38#128971519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87684455-C-A

128973942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87687224-T-A

128974026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87687296-A-G

128974343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87687541-C-T

128975602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87688974-A-T

http://identifiers.org/hco/3/GRCh38#128975646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87689013-C-A

128975646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87689013-C-T

128975700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87689053-G-A

128975700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87689053-G-T

http://identifiers.org/hco/3/GRCh38#128976507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87689854-C-A

http://identifiers.org/hco/3/GRCh38#128976837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87690145-C-A

128976837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690145-C-T

http://identifiers.org/hco/3/GRCh38#128976838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87690146-C-A

http://identifiers.org/hco/3/GRCh38#128976859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87690166-A-C

http://identifiers.org/hco/3/GRCh38#128976899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87690203-A-C

128976920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690222-G-A

128976920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690222-G-T

128977023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87690328-C-T

128977047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87690352-G-A

128977047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87690352-G-C

128977093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690395-G-A

128977093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690395-G-C

128977093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690395-G-T

128977161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690456-A-G

128977316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690592-T-A

128977375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690659-G-C

128977383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690667-T-C

128977496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690694-C-T

128977577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690761-G-A

128977618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690795-G-C

128977618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690795-G-T

128977719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690882-T-C

128977730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690894-G-A

128977730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690894-G-T

128977772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87690921-T-G

http://identifiers.org/hco/3/GRCh38#128977899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87691011-C-A

128977899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691011-C-T

http://identifiers.org/hco/3/GRCh38#128977933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87691033-C-A

128977933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691033-C-T

128977973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691062-A-G

128978042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691102-C-G

128978042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691102-C-T

128978072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87691132-T-C

128978123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87691183-T-C

128987355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87694072-T-C

128987626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87694860-A-G

http://identifiers.org/hco/3/GRCh38#128987689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: http://identifiers.org/mco/6/GRCm39#87694923-C-A

128987735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87694969-T-C

128987887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87695114-G-A

128987887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87695114-G-T

128987917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87695140-C-G

128987917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87695140-C-T

http://identifiers.org/hco/3/GRCh38#128987929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87695159-C-A

128987929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87695159-C-T

128987930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87695160-G-A

128987930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87695160-G-T

128987993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87695234-G-A

128988033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87695271-T-A

128988033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87695271-T-C

http://identifiers.org/hco/3/GRCh38#128988723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87695746-C-A

128988723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87695746-C-T

128992910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87698712-G-A

128992910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87698712-G-T

128992932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87698734-T-G

128993342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 87699093-A-G

http://identifiers.org/hco/3/GRCh38#128993418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87699141-C-A

128993418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699141-C-T

128993504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699221-T-C

128993510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699227-T-A

128993510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699227-T-C

128993664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699398-A-G

http://identifiers.org/hco/3/GRCh38#128993688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87699444-C-A

128993688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699444-C-T

http://identifiers.org/hco/3/GRCh38#128993692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87699448-C-A

128993692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699448-C-T

128993696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699452-G-A

128993696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699452-G-T

128993719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699478-T-C

128993719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699478-T-G

128993723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699482-T-G

128993732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699491-G-A

128993732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699491-G-T

128993741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87699500-G-A

128993741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87699500-G-T

128993759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87699518-A-G

http://identifiers.org/hco/3/GRCh38#128993865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87699593-C-A

128993865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87699593-C-T

128993921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699624-G-A

128993921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699624-G-T

128994064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699722-A-G

128994090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699749-G-A

128994090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699749-G-C

128994120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87699775-A-G

128994742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87700380-G-A

128994997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87700634-C-T

http://identifiers.org/hco/3/GRCh38#128995030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87700650-C-A

128995189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87700813-T-C

128995301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87700920-C-T

128995399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87701000-A-T

128995535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87701129-C-G

128995535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87701129-C-T

128995578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87701172-C-T

128999029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702892-G-A

128999054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702917-T-G

128999504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87703353-A-T

http://identifiers.org/hco/3/GRCh38#128999512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87703361-C-A

128999512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87703361-C-T

129000918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87707431-T-C

129000920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87707433-T-A

129001145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87707510-C-T

129001157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87707522-G-A

129001157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87707522-G-T

129001402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707675-G-A

129001476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707745-C-G

129001476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707745-C-T

129001484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707753-G-A

129001484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707753-G-C

129001503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707771-G-A

129001503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707771-G-C

129001503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707771-G-T

129001519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707787-G-T

129001520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707788-A-G

http://identifiers.org/hco/3/GRCh38#129001522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87707790-C-A

129001522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707790-C-T

129001578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707830-G-A

129001578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707830-G-T

http://identifiers.org/hco/3/GRCh38#129001584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87707836-A-C

129001584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707836-A-T

http://identifiers.org/hco/3/GRCh38#129001601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87707845-C-A

129001601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707845-C-T

129001653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707864-G-A

129001653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 87707864-G-T

http://identifiers.org/hco/3/GRCh38#129001654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87707865-A-C

129001654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707865-A-G

129001655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87707866-G-A

129001655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707866-G-C

129001655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707866-G-T

http://identifiers.org/hco/3/GRCh38#129001854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708067-C-A

129001854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708067-C-G

129001854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708067-C-T

129001877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87708090-C-T

http://identifiers.org/hco/3/GRCh38#129001884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708097-C-A

129001884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87708097-C-T

http://identifiers.org/hco/3/GRCh38#129001927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708128-C-A

129001927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708128-C-G

129001927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708128-C-T

129001935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708136-G-A

129001952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87708153-G-C

129001960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708161-G-A

129001960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708161-G-C

129001960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708161-G-T

129001975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708176-A-G

129001984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708185-C-T

http://identifiers.org/hco/3/GRCh38#129002037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708238-C-A

129002037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708238-C-G

129002037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708238-C-T

http://identifiers.org/hco/3/GRCh38#129002129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708330-C-A

129002129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708330-C-G

129002129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87708330-C-T

http://identifiers.org/hco/3/GRCh38#129002138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708339-C-A

129002138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87708339-C-G

http://identifiers.org/hco/3/GRCh38#129002150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708351-C-A

http://identifiers.org/hco/3/GRCh38#129002177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708378-C-A

129002177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 87708378-C-T

129002205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87708403-A-G

129002205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87708403-A-T

http://identifiers.org/hco/3/GRCh38#129002225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708423-C-A

129002225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 87708423-C-G

129002225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 87708423-C-T

129002267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708465-G-T

http://identifiers.org/hco/3/GRCh38#129002309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708507-C-A

129002369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708535-G-A

129002369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708535-G-C

129002369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708535-G-T

129002371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708537-T-C

129002425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708543-G-A

129002425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708543-G-C

129002428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708546-G-A

129002488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87708604-T-C

http://identifiers.org/hco/3/GRCh38#129002510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708625-C-A

129002510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87708625-C-T

http://identifiers.org/hco/3/GRCh38#129002620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708680-A-C

129002620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708680-A-G

129002644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708703-T-A

129002702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708740-G-T

129002713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708751-G-A

129002713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708751-G-T

129003365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87709318-A-G

129003494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87709451-G-A

129003718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87709612-G-A

129003887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87709728-C-T

129004123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87709977-C-G

129004936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87710468-G-A

129005232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87710709-A-T

129005436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87710898-C-T

129005972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87711422-C-T

129006051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87711499-A-G