60091923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 72582891-G-A

60091923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 72582891-G-T

60091926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 72582894-T-A

60091926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 72582894-T-C

60091926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 72582894-T-G

http://identifiers.org/hco/14/GRCh38#60092002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#72582947-C-A

60092002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72582947-C-G

http://identifiers.org/hco/14/GRCh38#60092010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#72582955-C-A

60092010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72582955-C-T

http://identifiers.org/hco/14/GRCh38#60092019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#72582971-C-A

60092019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72582971-C-G

60092019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72582971-C-T

60092043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72582993-G-T

60092092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72583031-T-C

http://identifiers.org/hco/14/GRCh38#60092110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#72583043-C-A

60092110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72583043-C-T

60092111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72583044-G-A

60092111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72583044-G-C

60092114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72583052-A-G

60092122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72583060-C-T

60092127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72583065-G-T

60092201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72583132-A-G

60092215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72583145-G-A

60092270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72583197-G-A

60092270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72583197-G-T

60092290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72583208-G-A

60092290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 72583208-G-T

60092292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72583210-C-G

60092292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72583210-C-T

http://identifiers.org/hco/14/GRCh38#60092333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72583229-C-A

60092333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72583229-C-T

60092339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72583235-G-A

60092362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72583257-T-A

60092362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72583257-T-C

60092391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72583285-G-T

http://identifiers.org/hco/14/GRCh38#60092392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72583286-C-A

60092392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72583286-C-T

60092409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72583303-G-T

60092563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72583446-A-G

60092767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72583696-T-C

60093490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72584420-G-A

60093544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72584458-A-G

60093583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72584497-A-G

60093641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72584539-A-G

60093661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72584557-T-G

60093889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72584778-A-G

60093956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72584831-C-T

60094207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72585046-G-A

60102440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72585430-G-A

60102493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72585480-A-G

60102915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72585857-T-G

60102972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72585911-G-T

60103072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72586027-T-C

60103218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72586136-G-C

60103438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72586355-T-G

60103539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72586470-A-G

60107500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72588063-G-A

60107500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72588063-G-T

60107521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72588085-G-A

60107521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72588085-G-T

60107565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72588130-T-C

http://identifiers.org/hco/14/GRCh38#60107809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72588373-C-A

60107809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72588373-C-G

60107809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72588373-C-T

60107815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72588379-A-G

60107851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72588415-T-C

60107857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72588421-A-G

60108505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72589079-G-A

60108505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72589079-G-T

60108531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72589106-T-A

60108531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72589106-T-G

http://identifiers.org/hco/14/GRCh38#60108567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72589142-C-A

60108636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72595922-G-A

60108636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72595922-G-C

60108639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72595925-A-G

60108730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596018-T-C

60108828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596101-C-T

60108830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596103-G-T

http://identifiers.org/hco/14/GRCh38#60108844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72596112-C-A

60108879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596134-C-T

60109021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596259-G-A

60109041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596279-G-T

60109105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596336-G-T

60109199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596413-T-C

60109217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596428-A-G

60109295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596514-T-C

60109295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596514-T-G

60109722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596646-T-C

60109729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596653-T-C

60109832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596706-T-C

60109855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596730-A-G

60109952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596831-G-A

60109952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596831-G-C

60109979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72596858-G-T

http://identifiers.org/hco/14/GRCh38#60110018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72596888-C-A

http://identifiers.org/hco/14/GRCh38#60110101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72596946-A-C

60110181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72597046-G-A

60110181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72597046-G-T

60110337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72597184-T-C

http://identifiers.org/hco/14/GRCh38#60110540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72597377-A-C

60110540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72597377-A-G

60110540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72597377-A-T

60110606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72597449-C-T

60110663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72597505-A-G

60110679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72597521-G-A

60110681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72597523-T-C

60110682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72597524-T-C

http://identifiers.org/hco/14/GRCh38#60110687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72597529-C-A

60110752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72597632-A-G

http://identifiers.org/hco/14/GRCh38#60111120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72598722-C-A

60111120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72598722-C-T

60111180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72598793-T-C

60111354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72598930-C-T

60111402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72599077-G-C

60111402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72599077-G-T

60111502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72599159-A-G

60111743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72600112-G-A

60111768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72600132-G-A

60111914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72600295-A-G

60111915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72600296-A-G

60111970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72600372-G-A

60111999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72600397-G-C

60111999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72600397-G-T

60112122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72600482-A-G

60112398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72600753-C-T

60112399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72600754-A-G

60112459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72600780-G-T

60112487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72600808-A-T

60112882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72601213-T-G

60113703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72601391-G-A

60113718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72601406-A-G

60113775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72601462-G-A

http://identifiers.org/hco/14/GRCh38#60113778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72601465-A-C

60113778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72601465-A-G

60114217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72601832-T-C

60114369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72601960-T-C

60114427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72602008-A-G

60114460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72602038-A-G

60114583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72602129-T-A

60114583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72602129-T-G

http://identifiers.org/hco/14/GRCh38#60114677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72602185-A-C

60114696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72602207-A-G

60114696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72602207-A-T

60114993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72602637-A-G

60115085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72602729-G-A

60115132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72602803-T-C

60115152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72602823-C-T

60115195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72602866-T-A

60115294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72602965-T-C

60115335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72603006-G-A

60115335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72603006-G-T

60115478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72603145-T-C

60115478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72603145-T-G

http://identifiers.org/hco/14/GRCh38#60115580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72603226-A-C

60115580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72603226-A-G

60115602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72603241-G-T

http://identifiers.org/hco/14/GRCh38#60115732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72603370-C-A

60115732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72603370-C-G

60115831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72603469-A-G

60115851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72603488-C-G

60115856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72603493-G-A

60115856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72603493-G-T

60115926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72603560-A-G

60115926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72603560-A-T

60115935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72603569-C-T

60116069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72603703-G-A

60116125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72603780-G-A

60116299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72603955-T-C

60118310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72613652-A-G

http://identifiers.org/hco/14/GRCh38#60118787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72614168-A-C

60118787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72614168-A-G

60118800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72614174-A-G

http://identifiers.org/hco/14/GRCh38#60118963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72615579-C-A

60118976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72615593-A-G

60120372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72615754-C-T

60121079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72616365-T-G

60121181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72616477-T-A

60121181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72616477-T-C

60121181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72616477-T-G

http://identifiers.org/hco/14/GRCh38#60121309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72616604-C-A

60121359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72616655-G-T

http://identifiers.org/hco/14/GRCh38#60121374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72616670-A-C

60121374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72616670-A-G

60122552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72618157-C-T

http://identifiers.org/hco/14/GRCh38#60122586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72618179-C-A

60122586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72618179-C-G

60122586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72618179-C-T

60122714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72618239-G-A

60122838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72618349-T-C

60122920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72618430-G-A

60122972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72618465-G-A

60123035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72618526-C-G

60123431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72619432-A-G

60123835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72619889-C-G

60124133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72620182-G-A

60124133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72620182-G-T

60124138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72620187-T-A

60124140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72620189-T-C

60124140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72620189-T-G

60124145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72620193-A-G

60124145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72620193-A-T

60124161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72620209-G-A

60124161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72620209-G-T

60124183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72620231-A-T

60124283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72620329-A-G

60124448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72620494-C-G

60124491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72620537-A-G

60124549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72620592-T-G

60124740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72620768-G-A

60124880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72620908-T-C

60124901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72620929-A-G

http://identifiers.org/hco/14/GRCh38#60124928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72620956-C-A

60125018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72621046-T-C

http://identifiers.org/hco/14/GRCh38#60125021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72621049-A-C

60125021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72621049-A-G

60125038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72621063-A-G

60125108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 72621133-T-G

60125198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72621223-G-A

60125365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72621362-T-A

60125396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72621377-T-G

60125436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72621412-G-A

http://identifiers.org/hco/14/GRCh38#60125493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72621468-C-A

60125493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72621468-C-T

60125569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72622060-A-G

60125596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72622089-A-G

60125643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72622134-T-C

60125790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72622281-A-G

60125865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72622342-A-G

60125887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72622359-G-A

60125890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72622362-T-G

60125917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72622385-G-A

60125917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72622385-G-C

60125921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72622389-T-C

60126003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72622468-A-G

http://identifiers.org/hco/14/GRCh38#60126062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72622526-C-A

60126062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72622526-C-T

60126094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72622551-G-A

60126223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72622693-G-T

60126228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72622699-G-A

60126228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72622699-G-T

http://identifiers.org/hco/14/GRCh38#60126252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72622723-C-A

60126252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72622723-C-G

60126307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72622783-A-G

60126316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72622792-G-T

60126353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72622829-T-C

60126353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72622829-T-G

60126408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72622889-G-A

60126678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72623136-G-T

60126855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72623294-A-G

60127068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72623502-T-A

60132682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72624737-G-T

60132856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72624954-A-G

60133150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72625280-T-G

60133197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72625326-G-C

60133531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72625588-G-T

60133739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72625908-G-A

60133739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72625908-G-T

60133756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72625931-A-G

60133756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72625931-A-T

60133816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72625988-G-T

60133845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72626017-T-G

60133848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72626020-T-G

60133857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72626025-G-A

60133858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72626026-A-G

60134017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 72626125-A-G

60134017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 72626125-A-T

60134068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 72626176-A-G

60134068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 72626176-A-T

http://identifiers.org/hco/14/GRCh38#60134158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72626266-A-C

60134337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72626439-G-T

60134374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72626477-T-C

http://identifiers.org/hco/14/GRCh38#60134496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72626588-A-C

60134496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72626588-A-G

60134496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72626588-A-T

60134521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72626610-G-T

60134653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72626740-T-A

60134775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72626862-A-T

60134779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72626866-A-G

http://identifiers.org/hco/14/GRCh38#60143747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72693901-C-A

60143843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72693988-T-C

http://identifiers.org/hco/14/GRCh38#60143845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72693990-C-A

60143845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72693990-C-T

http://identifiers.org/hco/14/GRCh38#60144681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72697044-A-C

60144681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697044-A-G

60144681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697044-A-T

60144696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697093-T-G

60144921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 72697304-T-C

60145154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697533-A-G

60145211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697589-G-T

60145212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697590-A-G

60145275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697663-C-T

60145351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697752-A-G

60145395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697779-G-A

60145395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697779-G-T

60145427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697797-A-T

60145442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697811-G-A

60145452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697821-G-A

60145458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697827-A-G

http://identifiers.org/hco/14/GRCh38#60145643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72697972-C-A

60145643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 72697972-C-T

http://identifiers.org/hco/14/GRCh38#60147803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72656848-C-A

60147857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72656885-T-A

60147857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72656885-T-C

60147904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72656924-G-A

60147904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72656924-G-T

60147906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72656926-T-C

http://identifiers.org/hco/14/GRCh38#60148799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72698762-C-A

60148813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72698776-T-C

http://identifiers.org/hco/14/GRCh38#60148893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72698839-A-C

60148911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72698857-T-A

60148911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72698857-T-C

60148911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72698857-T-G

60149382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72699038-T-C

60149410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72699066-G-A

60149473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72699129-A-G

60149603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72699261-A-G

60149636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72699294-T-A

60149636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72699294-T-C

60149639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72699297-A-G

60149639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72699297-A-T

http://identifiers.org/hco/14/GRCh38#60149640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72699298-A-C

http://identifiers.org/hco/14/GRCh38#60149644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72699302-C-A

60149644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72699302-C-T

60149713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72699370-T-C

60149929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72699690-G-A

60149929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72699690-G-T

60149941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72699711-G-T

60149984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72699767-T-C

60150083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72699893-T-C

60150089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72699899-A-G

60150137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72699947-T-C

60150137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72699947-T-G

http://identifiers.org/hco/14/GRCh38#60150195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72700005-A-C

60150195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72700005-A-G

http://identifiers.org/hco/14/GRCh38#60150197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72700007-A-C

60150197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72700007-A-G

60150197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72700007-A-T

60150233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72700055-G-A

60150233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72700055-G-T

60150248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72700066-A-G

http://identifiers.org/hco/14/GRCh38#60152105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72702290-A-C

60152105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702290-A-T

60152124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702308-G-C

60152180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702361-A-G

60152306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702469-G-A

60152365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702529-C-G

60152570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702702-G-A

60152570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702702-G-C

60152570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702702-G-T

60152572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702704-A-T

http://identifiers.org/hco/14/GRCh38#60152579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72702711-C-A

60152579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702711-C-G

60152579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702711-C-T

http://identifiers.org/hco/14/GRCh38#60152580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72702712-C-A

60152580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702712-C-T

http://identifiers.org/hco/14/GRCh38#60152590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72702746-C-A

60152590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702746-C-G

60152590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702746-C-T

http://identifiers.org/hco/14/GRCh38#60152610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72702765-A-C

60152610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72702765-A-G

http://identifiers.org/hco/14/GRCh38#60152636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72702791-A-C

60152847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72702981-T-C

60152855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72702989-C-T

60153225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72703341-G-A

60153798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72703922-A-G

60153836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72703975-T-A

60153836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72703975-T-C

60153899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72704035-T-C

60154168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72704310-T-C

60154176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72704358-G-T

http://identifiers.org/hco/14/GRCh38#60154196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72704375-C-A

60154196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72704375-C-T

60154446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72704758-G-C

60154596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72704907-G-C

60154694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72705013-A-G

60154712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72705035-C-T

60154888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72705211-A-G

http://identifiers.org/hco/14/GRCh38#60155679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72705768-C-A

60155756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72705837-T-A

60155757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72705838-A-G

http://identifiers.org/hco/14/GRCh38#60155773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72705857-C-A

60155820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72705902-G-A

60155820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72705902-G-T

60155883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72705969-T-C

http://identifiers.org/hco/14/GRCh38#60155913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72706037-C-A

60155913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72706037-C-T

60155940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72706061-T-A

60155961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72706079-A-G

60156046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72706164-T-C

60156046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72706164-T-G

60156097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72706215-A-G

60156226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72706361-A-G

60156234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72706369-G-A

60156234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72706369-G-T

http://identifiers.org/hco/14/GRCh38#60156247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72706382-C-A

60156247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72706382-C-T

http://identifiers.org/hco/14/GRCh38#60156248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72706383-C-A

http://identifiers.org/hco/14/GRCh38#60156294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72706436-C-A

http://identifiers.org/hco/14/GRCh38#60156303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72706445-C-A

60156303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72706445-C-T

http://identifiers.org/hco/14/GRCh38#60156334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72707069-C-A

60156336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72707071-T-A

60156372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72707120-G-A

60157366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72649983-C-T

http://identifiers.org/hco/14/GRCh38#60157562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72708561-C-A

60157562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72708561-C-T

60157683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72708674-A-G

http://identifiers.org/hco/14/GRCh38#60157824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72708861-C-A

60157824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72708861-C-G

60158339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72650698-C-T

60158359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72650708-A-G

60158390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72650737-A-T

60163804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72710189-G-A

http://identifiers.org/hco/14/GRCh38#60163995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72710361-A-C

http://identifiers.org/hco/14/GRCh38#60164019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72710393-A-C

60164029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72710403-C-T

http://identifiers.org/hco/14/GRCh38#60164305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#72710589-C-A

60164340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72710623-A-G

60164412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72710683-G-A

60164687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72711024-A-T

60164825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72711126-C-T

http://identifiers.org/hco/14/GRCh38#60164843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#72711134-A-C

60165035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72711324-G-A

60165035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72711324-G-C

60165035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72711324-G-T

60165086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72711348-G-A

60165086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72711348-G-T

60165111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72711362-C-T

60165223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 72711449-G-A

60165226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 72711452-A-T

60165234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72711460-G-T

60165276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72711502-G-A

60165276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72711502-G-T

http://identifiers.org/hco/14/GRCh38#60165326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#72711554-C-A

60165326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72711554-C-G

60165326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72711554-C-T

60165328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72711556-G-A

60165328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72711556-G-C

60165328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72711556-G-T

60165332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72711560-G-A

60165332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72711560-G-T

60165702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72714784-G-A

60165746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72714818-G-C

60165746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72714818-G-T

60165791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72714868-G-A

60166080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72715126-A-G

60166261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72715276-G-A

60166294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20349
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72715309-G-C