37511209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 45034552-G-A

37511209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 45034552-G-T

http://identifiers.org/hco/9/GRCh38#37511210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#45034553-C-A

37511210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 45034553-C-T

37511261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45034605-G-A

37511261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45034605-G-T

37511305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45034628-G-A

37511305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45034628-G-C

http://identifiers.org/hco/9/GRCh38#37511333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45034654-C-A

37511333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45034654-C-T

http://identifiers.org/hco/9/GRCh38#37511544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45034841-C-A

37511544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45034841-C-T

37511576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45034892-G-A

37511576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45034892-G-T

37511587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45034903-G-A

37511687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035014-G-A

37511830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035185-T-C

37511837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035192-G-C

37511837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035192-G-T

http://identifiers.org/hco/9/GRCh38#37511884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45035232-C-A

37511884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035232-C-G

37511884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035232-C-T

http://identifiers.org/hco/9/GRCh38#37511912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45035272-C-A

37511912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035272-C-G

37511912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035272-C-T

37512015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035373-G-T

37512080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035441-T-C

37512103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035461-G-A

37512124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035481-G-T

37512167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035508-A-G

37512167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035508-A-T

37512200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035537-C-T

http://identifiers.org/hco/9/GRCh38#37512285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45035624-C-A

37512409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035748-T-C

http://identifiers.org/hco/9/GRCh38#37512440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45035780-C-A

37512462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035807-A-G

37512462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035807-A-T

http://identifiers.org/hco/9/GRCh38#37512478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45035825-C-A

37512478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3 prime UTR variant
orthologous variants: 45035825-C-G

37512598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: synonymous variant
orthologous variants: 45035959-C-G

37512598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: synonymous variant
orthologous variants: 45035959-C-T

37512688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: synonymous variant
orthologous variants: 45036049-T-C

37512691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: synonymous variant
orthologous variants: 45036052-T-C

37512715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: missense variant
orthologous variants: 45036076-A-T

37512755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: intron variant
orthologous variants: 45036112-G-T

http://identifiers.org/hco/9/GRCh38#37512765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45036117-C-A

37512765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: intron variant
orthologous variants: 45036117-C-T

37512775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: intron variant
orthologous variants: 45036126-T-C

37512775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: intron variant
orthologous variants: 45036126-T-G

37512789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: intron variant
orthologous variants: 45036136-A-G

37512789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: intron variant
orthologous variants: 45036136-A-T

37512861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: intron variant
orthologous variants: 45036207-G-A

37512861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: intron variant
orthologous variants: 45036207-G-C

37512861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: intron variant
orthologous variants: 45036207-G-T

37516123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45040745-T-A

37516123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45040745-T-C

37516163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45040780-G-A

37516163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45040780-G-C

37516163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45040780-G-T

http://identifiers.org/hco/9/GRCh38#37516195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45040812-C-A

37516195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45040812-C-G

37516195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45040812-C-T

37516226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45040844-A-G

37516228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45040846-G-A

37516228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45040846-G-T

37516457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45041041-G-A

37517550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45041247-G-T

37517582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45041275-C-G

37518374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 45041981-A-G

http://identifiers.org/hco/9/GRCh38#37518496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45042091-A-C

37518496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45042091-A-G

http://identifiers.org/hco/9/GRCh38#37518513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45042111-C-A

37518841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45042344-T-C

37518928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45042440-G-T

http://identifiers.org/hco/9/GRCh38#37519055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45042555-A-C

37519055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45042555-A-G

37519055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45042555-A-T

37519067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45042567-G-A

37521557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45043628-G-A

37521557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45043628-G-T

37521903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 45043970-T-A

37521903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 45043970-T-C

37521924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45043987-C-T

37522003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45044030-A-T

37522155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45044146-G-A

37522290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45044254-G-C

37522300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45044264-A-G

37522392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45044332-A-T

37522393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45044333-G-T

http://identifiers.org/hco/9/GRCh38#37522416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45044356-C-A

37522416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45044356-C-G

37522416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45044356-C-T

http://identifiers.org/hco/9/GRCh38#37522423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45044363-C-A

37522423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45044363-C-T

http://identifiers.org/hco/9/GRCh38#37522578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45044487-C-A

37522578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45044487-C-T

37522643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45044536-A-G

37522704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45044575-T-A

37522704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45044575-T-G

37522709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45044580-G-T

37522789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45044662-C-T

37522817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45044708-C-T

37522928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45044819-T-C

http://identifiers.org/hco/9/GRCh38#37523004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45044891-C-A

http://identifiers.org/hco/9/GRCh38#37523021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45044908-C-A

37523021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45044908-C-T

37523089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45044985-T-C

http://identifiers.org/hco/9/GRCh38#37523092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45044988-C-A

37524353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45045599-G-A

37524402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45045663-C-T

http://identifiers.org/hco/9/GRCh38#37524431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45045691-C-A

37524436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45045696-C-T

37524449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45045709-T-C

37524663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45045954-G-C

37524775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45046055-C-T

37524794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45046073-G-A

37524794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45046073-G-C

37524850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45046123-A-G

37524853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45046126-G-A

http://identifiers.org/hco/9/GRCh38#37524978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45046220-C-A

37524978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45046220-C-T

37525007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45046241-T-G

37525052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45046276-C-T

http://identifiers.org/hco/9/GRCh38#37525060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45046284-C-A

http://identifiers.org/hco/9/GRCh38#37525277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45046554-C-A

37525277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45046554-C-T

http://identifiers.org/hco/9/GRCh38#37525282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45046559-A-C

37525314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45046594-G-A

37525314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45046594-G-T

37525418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45046756-G-C

37526454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45047147-A-G

37528073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45047373-A-G

37528147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45047411-T-C

37528205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45047443-T-C

37528527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45047782-C-T

37528692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45047940-A-G

37528976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45048281-A-G

37529033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45048336-T-G

37529243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45048559-A-G

http://identifiers.org/hco/9/GRCh38#37529338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45048644-C-A

http://identifiers.org/hco/9/GRCh38#37529357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45048663-C-A

37529404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45048713-G-A

37529404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45048713-G-C

37529437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45048769-C-T

37529438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45048770-A-G

37529667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45049040-C-T

37529683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45049056-G-A

37529698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45049071-G-A

37529767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45049137-G-A

37529767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45049137-G-T

http://identifiers.org/hco/9/GRCh38#37529862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45049226-C-A

37531458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45051171-A-G

37531565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45051253-T-C

37531794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45051462-G-A

37531794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45051462-G-T

37531888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45051529-T-C

37531900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45051541-A-G

37531918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45051562-T-C

http://identifiers.org/hco/9/GRCh38#37531933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45051577-C-A

37531933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45051577-C-T

37532055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45051699-T-C

37532073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45051717-G-C

http://identifiers.org/hco/9/GRCh38#37532078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45051722-C-A

37536818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45058024-T-C

37536918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45058114-C-G

37536979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45058177-G-A

37536979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45058177-G-T

37537063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45058230-C-T

37537066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45058233-A-G

37537067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45058234-T-C

http://identifiers.org/hco/9/GRCh38#37537073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45058240-C-A

37537158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 45058377-G-A

37537182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 45058401-G-A

37537182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 45058401-G-T

37537200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 45058419-G-A

37537380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 45058599-A-G

37537632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 45058839-G-C

37537660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 45058867-T-C

37537818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 45059025-G-A

37537975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45059180-G-A

37537975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45059180-G-C

37538005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45059216-G-A

37538005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45059216-G-C

37538005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45059216-G-T

37538235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45059451-C-T

37538236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45059452-C-T

37538616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45059962-G-T

37538692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45060069-A-G

http://identifiers.org/hco/9/GRCh38#37538727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45060121-C-A

37538727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45060121-C-G

37538727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45060121-C-T

37538807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45060218-G-A

37539209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45060550-A-G

37539260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45060601-T-C

37539311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45060646-A-T

37539442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45060741-T-C

37539513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45060801-G-C

37539801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45061055-T-C

37539852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45061104-T-C

37540631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45061483-G-A

37540644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45061496-C-T

http://identifiers.org/hco/9/GRCh38#37541081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45061854-C-A

37541130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45061898-G-A

37541130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45061898-G-C

37541442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 45062198-G-A

37541442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 45062198-G-T

37541450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 45062206-G-A

37543377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45065616-G-A

37557713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45066259-T-C

37557794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45066315-T-C

37558196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45066685-G-C

37558599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45066988-A-G

37560055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45067933-G-A

http://identifiers.org/hco/9/GRCh38#37560292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45068166-C-A

37560749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45069465-T-C

37560818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45069516-G-T

http://identifiers.org/hco/9/GRCh38#37561546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45069729-A-C

37561692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45069866-A-G

http://identifiers.org/hco/9/GRCh38#37561851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45070104-A-C

37561857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45070110-G-A

37561967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45070197-A-T

37561982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45070212-T-G

37562011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45070241-C-T

37562078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45070298-C-T

http://identifiers.org/hco/9/GRCh38#37565611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45071670-C-A

37566024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45071973-A-G

37566096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45072026-C-T

http://identifiers.org/hco/9/GRCh38#37566102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45072032-C-A

37566102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45072032-C-G

37566102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45072032-C-T

37566117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45072050-C-G

37566166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45072093-G-A

37566333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45072169-C-T

37566483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45072357-A-T

http://identifiers.org/hco/9/GRCh38#37566554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45072429-A-C

37566666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45072529-C-G

37566911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45072752-T-C

37567063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45072901-A-G

37567763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45075033-C-T

37567959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45075206-C-T

37568032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45075275-T-C

http://identifiers.org/hco/9/GRCh38#37568039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45075280-A-C

37572532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45079921-C-G

37572532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45079921-C-T

37572633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45080018-G-A

37572876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45080251-T-C

37573021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-T

37573159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-C

37573159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-G

37573591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45081743-G-A

http://identifiers.org/hco/9/GRCh38#37574341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45082753-C-A

37574341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45082753-C-T

37575036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45083438-G-T

37575116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45083514-G-A

http://identifiers.org/hco/9/GRCh38#37575412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45083814-C-A

http://identifiers.org/hco/9/GRCh38#37575425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45083832-C-A

37575483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 45083869-T-C

http://identifiers.org/hco/9/GRCh38#37575521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45083976-C-A

http://identifiers.org/hco/9/GRCh38#37575568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45084025-C-A

37575839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45084220-T-C

37576070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45084384-T-C

37576187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45084467-A-G

37576188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 45084468-G-T

37576205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 45084484-G-A

37576205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13589
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 45084484-G-T