http://identifiers.org/hco/5/GRCh38#145441243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41657171-C-A

145450745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41663939-G-T

145450799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41663992-G-T

145450817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41664006-G-T

http://identifiers.org/hco/5/GRCh38#145450839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41664029-C-A

145450984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41664166-G-T

http://identifiers.org/hco/5/GRCh38#145451036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41664207-C-A

http://identifiers.org/hco/5/GRCh38#145451102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41664273-C-A

145451102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41664273-C-T

http://identifiers.org/hco/5/GRCh38#145451190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41664362-C-A

145451190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41664362-C-T

145451196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41664368-T-C

145451245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41664416-A-G

145467779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41675229-G-A

145467826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41675276-A-G

145469180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41675455-C-T

145469194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41675471-A-G

145469289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41675557-A-G

145469294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41675562-T-G

145469407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41675650-A-G

145469410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41675653-A-G

145469429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41675672-G-A

145469557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41675787-T-G

145469601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41675831-A-G

145469670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41675900-G-A

145469757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41676002-G-A

145469761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41676006-G-A

145469761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41676006-G-C

145469761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41676006-G-T

145469846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41676091-G-A

145469846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41676091-G-C

145470601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41676883-G-A

145470841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41677120-A-G

145471657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41678204-G-A

145471829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41678398-G-A

145471829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41678398-G-T

http://identifiers.org/hco/5/GRCh38#145471852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41678422-A-C

145471898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41678467-A-G

http://identifiers.org/hco/5/GRCh38#145471916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41678484-C-A

145471916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41678484-C-T

145471938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41678506-A-G

145472022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41678588-G-A

145472294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41678702-C-T

145472493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41678897-A-G

http://identifiers.org/hco/5/GRCh38#145473316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41679467-C-A

145473448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41679602-G-A

145473789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41679975-A-G

145474262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41692071-C-T

145474267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41692077-G-A

145474409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41692214-G-A

145474770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41692576-T-C

145474784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41692590-T-G

http://identifiers.org/hco/5/GRCh38#145474831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41692634-A-C

145475249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41693003-A-T

145475293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41693050-T-G

http://identifiers.org/hco/5/GRCh38#145475385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41693134-A-C

145475385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41693134-A-G

145475531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41694382-C-T

145475535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41694386-G-T

145475601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41694452-A-G

145475839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41694706-C-T

145476014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41694880-G-A

145476225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41695083-T-C

http://identifiers.org/hco/5/GRCh38#145476838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41695431-A-C

http://identifiers.org/hco/5/GRCh38#145476936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41695903-C-A

145476936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41695903-C-T

145476999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41695969-T-C

145477026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41695997-T-G

145477318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41696290-G-T

145477534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41696499-C-T

145477655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41696604-G-A

145477683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41696619-A-G

145477727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41696663-G-A

145479585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41696874-T-C

145479632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41696921-T-G

145480300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41697738-T-G

145480529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41697936-G-A

145480617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41698036-G-C

145480687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41698118-C-T

145480862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41698268-T-C

145481288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41700544-T-A

145481556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41700794-C-T

http://identifiers.org/hco/5/GRCh38#145481577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41700818-A-C

145483488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41701942-C-T

145483498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41701952-A-G

145483664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41702075-A-G

145483766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41702101-C-T

145483832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41702167-A-G

http://identifiers.org/hco/5/GRCh38#145484071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41702401-A-C

145484146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41702476-G-A

145484228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41702555-T-C

145484252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41702577-G-T

145484597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41702905-A-T

145484634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41702950-T-C

145485102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41703958-A-G

145485428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41704260-T-A

145485463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41704297-C-T

145485671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41704505-T-A

145485765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41704590-A-T

145485773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41704598-G-C

145485889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41704713-C-T

http://identifiers.org/hco/5/GRCh38#145485908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41704730-A-C

145486060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41704885-T-C

145488308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41708788-T-C

145488426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41708925-G-A

145489057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41709619-G-T

http://identifiers.org/hco/5/GRCh38#145489374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41709919-A-C

http://identifiers.org/hco/5/GRCh38#145489416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41709974-A-C

145489601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41710151-C-T

145489656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41710207-G-T

145489761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41710311-G-A

145489869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41710415-C-T

145490020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41710570-A-T

http://identifiers.org/hco/5/GRCh38#145490034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41710582-C-A

145490213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41711182-G-A

145490245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41711216-T-C

145490252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41711223-C-T

145490263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41711234-T-C

http://identifiers.org/hco/5/GRCh38#145490334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41711532-C-A

145490340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41711538-C-T

145490345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41711543-G-C

145490631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41711796-T-C

145490631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41711796-T-G

145490671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41711830-T-G

145490699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41711858-G-C

145490729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41711887-A-G

145490837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41711971-G-A

145490845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41711979-A-G

http://identifiers.org/hco/5/GRCh38#145490900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41712004-C-A

145490900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41712004-C-G

145490920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41712024-A-T

145493840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41713286-C-T

145493952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41713395-T-A

145493993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41713434-C-T

145494290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41713817-T-C

145494384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41713916-G-A

145494384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41713916-G-T

145494581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41714090-C-T

145494601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41714110-T-A

145494710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41714216-T-C

145494744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41714253-G-C

145494800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41721577-C-G

145494805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41721598-A-T

145494860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41721652-T-C

145494936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41721727-A-G

145495196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41721934-T-C

145495273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41722013-G-A

145495451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41722185-T-A

145495460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41722192-G-A

145495460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41722192-G-T

http://identifiers.org/hco/5/GRCh38#145495545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41722286-C-A

145495882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41722651-C-T

145496019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41722770-T-C

145496159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41722915-C-T

145496168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41722924-A-T

145496214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41722964-T-C

145496235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41722984-T-A

145496235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41722984-T-C

145496350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41723081-T-C

145496455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41723186-C-T

http://identifiers.org/hco/5/GRCh38#145496549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41723279-A-C

145496553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41723283-C-G

145496611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41723340-G-A

145496611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41723340-G-T

145497479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41725728-G-A

145497677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41725896-T-C

145497701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41725920-C-T

145497764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41725983-G-A

145497919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41726145-T-C

145498108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41726320-T-C

145498184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41726396-G-A

145498184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41726396-G-T

145498333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41726528-A-G

145498350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41726545-A-G

145499373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41726746-A-G

145499630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41728624-T-C

145499705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41728696-A-G

145499714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41728705-C-G

http://identifiers.org/hco/5/GRCh38#145500594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41729180-C-A

145500666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41729249-G-C

145500669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41729252-T-C

145500716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41729303-T-A

145500977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41729558-G-A

145501027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41729608-C-T

145501052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41729633-C-T

145501192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41729776-G-T

145501328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41730329-C-T

145502499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41740039-G-T

145502508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41740048-G-A

145502567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41740104-G-C

145502763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41740298-C-T

http://identifiers.org/hco/5/GRCh38#145502787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41740322-C-A

145502866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41740395-C-T

http://identifiers.org/hco/5/GRCh38#145502880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41740409-C-A

145502880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41740409-C-G

145502894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41740423-A-G

145503087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41740657-G-A

145503087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41740657-G-T

145503418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41740972-A-G

145503494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41741048-G-A

145504197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41743010-G-C

145504306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41743117-T-C

145504329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41743133-G-T

http://identifiers.org/hco/5/GRCh38#145504640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41743393-C-A

145504640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41743393-C-T

145504762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41743513-T-A

145504878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41743623-C-T

145505219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41744023-G-C

145505259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41744062-C-T

145505268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41744071-A-G

145505335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41744132-G-A

http://identifiers.org/hco/5/GRCh38#145505481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41744260-C-A

145505735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41744518-A-T

145505745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41744528-G-A

http://identifiers.org/hco/5/GRCh38#145505805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41744588-A-C

145505811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41744594-T-C

145505900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41744688-G-A

145505900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41744688-G-T

145505972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41744737-G-C

http://identifiers.org/hco/5/GRCh38#145507703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41745753-A-C

http://identifiers.org/hco/5/GRCh38#145507722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41745772-A-C

145508045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41746127-T-C

http://identifiers.org/hco/5/GRCh38#145508078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41746160-A-C

145508078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41746160-A-G

145508196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41746270-C-T

145508209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41746283-T-C

145508212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41746286-A-G

145508638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41753429-G-A

145509101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41754061-T-C

145509104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41754064-T-G

145509161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41754125-T-C

145509184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41754150-T-C

145509208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41754174-G-A

145509217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41754183-G-A

145509352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41754305-C-T

145509540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41754474-C-T

http://identifiers.org/hco/5/GRCh38#145509647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41754571-C-A

145509657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41754581-T-G

145509689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41754614-T-A

145510218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41755078-T-C

145510264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41755125-G-A

http://identifiers.org/hco/5/GRCh38#145510874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41755699-A-C

145511156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41755949-C-T

145511306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41756100-T-A

http://identifiers.org/hco/5/GRCh38#145511364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41756162-C-A

145511398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41756191-T-A

145511416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41756209-G-A

145518420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41759226-G-A

145518478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41759276-G-A

145518490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41759288-G-A

145518588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41759452-G-A

145518588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41759452-G-C

145518616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41759480-G-A

145518679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41759561-G-A

145518829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41759674-C-T

145518861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41759706-T-C

145518988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41759826-A-G

http://identifiers.org/hco/5/GRCh38#145519208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41760005-C-A

145519265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41760063-A-G

145519387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41760346-T-A

http://identifiers.org/hco/5/GRCh38#145519760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41760729-C-A

145519822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41760789-A-T

145519911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41760878-G-A

http://identifiers.org/hco/5/GRCh38#145520443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41761146-C-A

145520443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41761146-C-T

145520867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41761318-T-C

http://identifiers.org/hco/5/GRCh38#145520883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41761334-C-A

145520954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41761396-C-G

145520954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41761396-C-T

145521175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41761608-T-A

145521307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41761741-C-G

145521335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41761771-G-A

145521401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41761839-A-G

145521430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41761867-A-G

145521583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41761995-T-C

145524796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41766030-T-C

145525281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41766675-C-T

145525285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41766679-G-C

145525295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41766686-G-A

145525305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41766694-G-C

145525482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41766861-C-G

145525496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41766884-G-A

145525871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41767508-G-T

145525917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41767549-T-C

145525937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41767569-G-A

145525937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41767569-G-T

145526032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41767667-T-C

145526054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41767687-C-T

145526276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41767896-G-C

145527586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41768246-A-G

145527586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41768246-A-T

145527874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41768510-A-G

145527882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41768518-C-T

145527951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41768573-C-T

145528034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41768648-A-G

145528074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41768685-T-C

145528142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41768753-T-C

145528222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41768833-G-C

145528341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41768960-T-A

145528341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41768960-T-C

145528351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41768970-G-C

145528360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41768975-T-C

145528602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41769177-T-C

145528639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41769214-T-C

145528653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41769228-G-A

145528720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41769291-C-T

145528750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41769328-G-C

145528764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41769345-C-T

145529043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41769644-C-T

145529494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41770091-C-T

145529509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41770106-G-A

145529509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41770106-G-T

145529708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41770303-C-T

145529999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41770596-A-G

145530167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41774511-C-T

145530180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41774524-G-A

145531110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41774774-T-A

145531150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41774813-G-T

145531335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41774925-A-G

145531569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41775158-A-G

145531893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41775438-G-A

145532163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41775664-G-A

145532168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41775669-G-C

145532223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41775723-T-C

145532458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41776051-C-T

145533955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41776283-T-C

145533968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41776296-T-C

145534006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41776327-T-C

145534178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777579-C-T

145534234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777633-G-A

145534267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777675-T-C

145534304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777712-G-A

145534584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777985-T-C

145534810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778196-G-A

145534810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778196-G-C

http://identifiers.org/hco/5/GRCh38#145534815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41778201-A-C

145535126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778519-T-G

145535269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778664-A-G

145535481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41779310-T-C

http://identifiers.org/hco/5/GRCh38#145535516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41779345-A-C

145535645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41779465-G-C

145535733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41779557-G-A

145535754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41779578-T-C

145535782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41779599-G-A

145535897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41779715-T-A

145536064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41779884-T-C

145536106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41779927-T-C

145536708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41780554-G-A

145536720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41780566-T-C

145536721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41780567-G-A

145536928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41780785-C-T

145536987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41780847-A-T

145536990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41780850-A-T

145538467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41786487-C-T

145538484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41786505-A-T

http://identifiers.org/hco/5/GRCh38#145538497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41786518-A-C

http://identifiers.org/hco/5/GRCh38#145538538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41786568-A-C

145538538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41786568-A-G

145538586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41786612-T-C

145538686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41786708-C-T

145538778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41786816-G-C

145538877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41786913-G-A

145539058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41787103-G-A

145539154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41787180-A-G

145539691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41787700-C-T

145539965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41787946-G-A

145540033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41788601-G-A

145540081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41788650-T-C

145540114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41788683-T-C

145541872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41790436-C-G

145541944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41790686-C-T

145542164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41791012-G-A

145542183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41791017-C-T

145542312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41791149-T-A

145542488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41791440-C-T

145542515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41791469-G-A

145542628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41791578-G-A

145542639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41791589-T-C

145542840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41791727-T-G

145542923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41791809-C-T

145543177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41792042-A-G

145543205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41792070-G-C

http://identifiers.org/hco/5/GRCh38#145543908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41792669-C-A

145544103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41792861-G-A

145544190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41792949-T-A

145544190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41792949-T-C

145544208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41792967-C-T

145544337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41793085-T-A

145544341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41793089-T-C

145544412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41793156-T-C

145544498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41793239-A-T

145544567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41793276-G-T

http://identifiers.org/hco/5/GRCh38#145544585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41793294-C-A

145544653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41793358-G-A

145544653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41793358-G-C

145544695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41793400-T-A

145544695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41793400-T-C

145544738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41793443-T-C

145545223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41793909-C-T

145545238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41793924-T-A

145545362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41794037-A-G

145545364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41794039-G-A

http://identifiers.org/hco/5/GRCh38#145545424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41794099-C-A

145545424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41794099-C-T

145545706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41794455-G-T

145545767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41794524-G-A

145545863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41794612-G-C

145546575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41797473-A-G

145546654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41797520-G-A

145546654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41797520-G-C

145546669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41797535-G-A

145546833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41797637-A-T

145546835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41797639-T-C

http://identifiers.org/hco/5/GRCh38#145547011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41797800-C-A

145547011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41797800-C-T

http://identifiers.org/hco/5/GRCh38#145547027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41797816-C-A

145547217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41798005-C-T

http://identifiers.org/hco/5/GRCh38#145547331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41798108-C-A

145547331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41798108-C-T

145547348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41798125-T-C

145547547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41798297-T-A

http://identifiers.org/hco/5/GRCh38#145548134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41798868-C-A

145548299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41799025-G-A

http://identifiers.org/hco/5/GRCh38#145548539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41800087-A-C

145548557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41800104-A-G

145548632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41800179-T-C

145548892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41800440-A-T

145548911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41800463-C-T

145548927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41800479-T-C

145549063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41800623-C-G

145549400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41801015-A-G

145550706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41801194-G-A

145550777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41801246-C-T

145551099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41801551-G-A

145551481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41801655-T-C

145551653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41801828-G-A

145551766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41801943-A-T

145551865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802038-G-C

145551889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802071-C-T

145551979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802094-C-T

http://identifiers.org/hco/5/GRCh38#145552125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41802239-C-A

145552146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802258-G-A

145552163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802275-A-G

145552175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802290-C-T

145552294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802389-C-T

145552319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802411-C-T

145552412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802507-C-T

145552442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802517-G-T

145552514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802582-C-T

145552580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802640-T-C

145552824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802843-C-G

145552837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802856-A-G

http://identifiers.org/hco/5/GRCh38#145553084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41803070-C-A

145553173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41803154-T-G

145553282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41803278-G-A

145553439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41803428-G-A

145553439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41803428-G-T

145553505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41803488-T-C

145553848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41804581-T-G

145554009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41804718-G-A

145554065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41804779-G-A

145554065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41804779-G-C

145554077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41804791-C-T

145554477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41805183-C-T

145554500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41805348-G-A

145554500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41805348-G-C

http://identifiers.org/hco/5/GRCh38#145554518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#41805366-A-C

145554523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41805371-G-T

http://identifiers.org/hco/5/GRCh38#145554525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#41805373-C-A

http://identifiers.org/hco/5/GRCh38#145554648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#41805583-C-A

145554652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41805587-G-A

145554875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41805801-G-A

http://identifiers.org/hco/5/GRCh38#145556755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41807787-C-A

145556937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41807957-A-G

145556987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41808005-G-A

145557068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41808081-G-T

145557126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41808143-T-C

145557882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41808680-G-A

145557882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41808680-G-T

145557912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41808722-T-C

145558137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41808861-T-C

145558202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41808926-G-T

145558430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41809158-G-A

145558569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41809297-G-A

http://identifiers.org/hco/5/GRCh38#145558866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41809597-A-C

145560412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41811510-G-A

145560539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41811632-G-A

145560829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41811924-G-A

145561002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41812097-T-C

145561002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41812097-T-G

145561115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41812204-G-A

145561115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41812204-G-T

145561629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41812675-G-T

145561642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41812688-T-C

145565303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41814582-A-G

145565404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41814680-C-T

145566115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41815251-C-T

145566222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41815354-C-T

145566248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41815380-T-G

145566446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41815605-G-A

145568066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41816151-G-A

145568150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41816238-G-C

145568317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41816383-T-C

145568412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41816476-C-T

145569233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41817325-T-A

145569233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41817325-T-C

145569433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41817510-C-T

145569492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41817562-T-C

http://identifiers.org/hco/5/GRCh38#145569504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41817573-A-C

145569640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41817708-C-T

http://identifiers.org/hco/5/GRCh38#145570016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41818680-C-A

145570016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41818680-C-T

145570072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41818750-T-C

145570172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41818849-C-T

145570188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41818865-C-T

145570428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41819116-A-T

145570430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41819118-T-A

145570430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41819118-T-C

145570432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41819120-T-A

145570447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41819134-T-A

145570479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41819164-T-G

http://identifiers.org/hco/5/GRCh38#145570721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41819389-C-A

145570813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41826577-C-T

http://identifiers.org/hco/5/GRCh38#145570930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41826685-C-A

145570995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41826741-C-T

145571030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41826776-G-A

145571034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41826780-G-T

145571208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41826932-C-T

http://identifiers.org/hco/5/GRCh38#145572610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41827140-C-A

145572753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41827279-A-G

145572845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41827368-C-T

145572887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41827412-T-C

145572891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41827416-G-T

http://identifiers.org/hco/5/GRCh38#145572920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41827448-A-C

145572920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41827448-A-G

145573209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41827624-G-A

145575230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41828335-A-G

145575259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41828364-T-G

145575420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41828519-G-A

145575518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41828615-G-A

145575554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41828631-T-C

145575606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41828682-G-A

http://identifiers.org/hco/5/GRCh38#145575673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41828748-C-A

145575697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41828772-T-C

145575719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41828790-A-G

145575725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41828796-C-G

145575792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41828863-C-T

145575940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41828999-G-A

145576016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41829062-T-A

145576016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41829062-T-C

145576019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41829065-C-T

145576055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41829098-A-G

145576254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41829288-A-G

145576288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41829322-T-C

145576353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41829381-T-A

145576353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41829381-T-G

145576365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41829393-T-C

145576407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41829438-C-T

145578165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41830488-G-A

145578171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41830494-G-T

http://identifiers.org/hco/5/GRCh38#145578183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41830506-C-A

145578294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41830614-C-T

145578449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41830771-C-T

145578472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41830794-G-T

145578596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41830925-T-G

145578810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41831132-G-T

145578829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41831150-T-C

145578978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41831373-A-T

145579044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41831462-T-C

145579196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41831613-C-T

145579414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41831803-T-C

145579691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41832078-T-C

http://identifiers.org/hco/5/GRCh38#145579745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41832131-C-A

145579860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41832250-G-C

145579884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41832267-A-G

145579943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41832354-G-A

145580137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41832935-G-C

145580175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41832973-A-G

http://identifiers.org/hco/5/GRCh38#145580222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41833018-A-C

145580222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41833018-A-G

145580528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41833304-G-A

145580545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41833321-G-C

145580633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41833418-G-T

145580725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41833515-C-T

145580833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41833608-C-T

145581010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41833787-T-C

145581014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41833790-T-G

145581232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41834000-C-G

145581542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41834585-C-G

145581545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41834589-G-A

http://identifiers.org/hco/5/GRCh38#145581552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41834596-C-A

145581616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41834660-T-G

145581760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41834813-G-A

http://identifiers.org/hco/5/GRCh38#145581845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41834898-C-A

145581864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41834917-G-T

http://identifiers.org/hco/5/GRCh38#145581906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41834959-C-A

145582022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41835076-T-A

145582100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41835195-G-A

145582155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41835249-G-T

145585787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839163-T-A

145586010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839355-G-A

145586010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839355-G-C

145586195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839526-C-T

145586198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839529-C-T

145586222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839552-T-G

http://identifiers.org/hco/5/GRCh38#145586288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41839618-A-C

145586335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839665-A-G

145586548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839740-C-G

145586567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839757-C-T

145586571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839761-T-C

145586671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839853-C-G

145586708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839878-G-A

145586765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839938-T-A

145586765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839938-T-C

145586873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41840001-C-T

145586945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41840056-G-A

145587003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41840117-C-T

http://identifiers.org/hco/5/GRCh38#145587042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41840164-A-C

145587121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41840245-G-C

145587245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41840371-A-G

145587300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41840414-G-A

145587362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41840465-C-T

145587372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41840475-T-C

http://identifiers.org/hco/5/GRCh38#145587416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41840519-A-C

145587441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41840544-A-G

145587470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41840573-G-A

145587558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41840661-T-C

http://identifiers.org/hco/5/GRCh38#145587559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41840662-A-C

145587658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41840761-T-A

145587661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41840764-C-G

145587753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41840856-G-T

145588119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41841198-C-G

145588119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41841198-C-T

145588276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841332-A-G

145588296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841353-T-C

145588296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841353-T-G

145588353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841409-G-T

145588382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841438-C-T

145588438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841493-C-T

145588478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841532-G-T

145588488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841542-C-T

145588698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841758-T-A

145588757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841841-G-T

145588771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841854-C-G

145588771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841854-C-T

145588782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841865-G-A

145588798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841881-G-T

145588830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841918-T-G

145588875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41841963-T-C

145588993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842062-T-G

145589083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842157-G-A

145589195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842277-T-C

145589448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842933-T-C

145589549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843012-A-T

145589556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843019-A-G

145589556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843019-A-T

145589596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843058-T-C

145589635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843092-A-G

145589686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843141-C-T

145589783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843233-C-T

145589887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843323-A-G

145589942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843378-T-C

145589998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843431-T-C

145589998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843431-T-G

145590030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843463-G-A

145590073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843502-A-G

145590374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41849593-T-C

145590424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41849639-A-G

145590521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41849711-A-G

145590544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41849728-A-G

http://identifiers.org/hco/5/GRCh38#145590770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41849914-C-A

145590836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41849951-A-G

145591429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41850249-T-C

145591721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41850518-A-G

145591786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41850574-T-C

145591924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41850692-A-G

145594606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41855213-G-A

http://identifiers.org/hco/5/GRCh38#145594635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41855241-A-C

145594636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41855242-T-C

http://identifiers.org/hco/5/GRCh38#145594696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41855306-A-C

145594704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41855316-G-C

145595845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41857798-G-T

http://identifiers.org/hco/5/GRCh38#145595917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41857865-C-A

145595922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41857870-C-G

145596716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860686-A-G

145596716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860686-A-T

http://identifiers.org/hco/5/GRCh38#145596947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41860879-C-A

145596976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860908-G-A

145596976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860908-G-C

145597036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860970-A-T

145597230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861169-T-C

http://identifiers.org/hco/5/GRCh38#145597247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41861186-A-C

145597385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861313-G-A

145597390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861322-C-G

145597407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861339-C-T

145597451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861380-A-G

http://identifiers.org/hco/5/GRCh38#145597557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41861478-C-A

145597627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862008-C-G

145597743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862110-G-C

145597743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862110-G-T

145597770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862132-T-G

145598171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862996-T-C

145598341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41863167-G-A

145598505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41863345-C-T

145598715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41863556-C-T

145599573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865407-A-G

145599654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865485-C-T

145599703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865525-G-A

145599947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865736-G-T

145628835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41872908-A-G

145628860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41872921-G-A

145628948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873010-A-T

145628998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873079-T-C

145629037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873119-G-A

145629037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873119-G-C

145629172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873246-G-A

145629197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873267-G-A

http://identifiers.org/hco/5/GRCh38#145629210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41873279-C-A

145629426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873493-T-C

145629444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873511-G-A

145629606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873639-G-T

http://identifiers.org/hco/5/GRCh38#145631564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41878412-C-A

145631564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41878412-C-T

http://identifiers.org/hco/5/GRCh38#145632224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41879017-C-A

145632224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41879017-C-G

145632224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41879017-C-T

145632954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880086-G-A

145633009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880141-T-C

145633117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880248-T-A

145633255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880341-C-T

145633315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880402-A-T

145633434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880524-A-G

145633535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880624-C-T

145633611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880686-G-A

145633780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880853-T-C

145633782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880855-T-C

145633867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880932-T-C

145633945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41881004-C-T

145634383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41881402-C-G

145634399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41881418-C-T

145634408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41881433-T-A

145634408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41881433-T-C

145634532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41881553-A-G

145634536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41881556-G-A

145634621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41881637-G-T

145635221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41882187-T-C

145635309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41882246-A-G

145635501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41882453-T-G

145635553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41882509-C-G

145635553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41882509-C-T

145635666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41882629-A-G

http://identifiers.org/hco/5/GRCh38#145635667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41882630-A-C

145635897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41882844-A-G

145636158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41883092-C-G

145636173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41883107-T-C

145636186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41883119-T-C

145636336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41883256-A-G

145636690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41883577-A-G

145636906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41883803-T-A

145636962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41883859-T-G

145636990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41883887-G-A

145637003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41883900-C-G

145637118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41883985-A-G

145637139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884006-T-A

145637139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884006-T-C

145637241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884102-T-A

145637241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884102-T-C

145637437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884283-T-A

145637448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884294-T-C

http://identifiers.org/hco/5/GRCh38#145637477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41884324-C-A

145637491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884338-A-G

145637626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884451-T-C

http://identifiers.org/hco/5/GRCh38#145637654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41884482-A-C

145637728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884538-T-C

145638207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884666-C-G

145638286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884740-A-G

145638329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884788-A-T

145638332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884791-C-T

145638390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884852-T-G

145638396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884858-C-T

145638500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884977-T-C

145638590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885058-T-G

145638723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885358-C-T

145638821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885478-G-A

145638823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885480-A-G

145638835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885492-A-G

145638857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885518-G-A

145638857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885518-G-T

http://identifiers.org/hco/5/GRCh38#145638904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41885565-C-A

145638904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885565-C-T

145638921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885582-C-T

145638922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885583-G-A

145638989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885643-G-T

145638990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885644-G-C

145639016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885649-T-C

145639016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885649-T-G

145656930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41887003-C-G

http://identifiers.org/hco/5/GRCh38#145656997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41887099-C-A

145657930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41887704-G-C

http://identifiers.org/hco/5/GRCh38#145657998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41887769-C-A

145657998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41887769-C-G

145658007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41887778-T-C

145658161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41887919-C-T

145658162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41887920-T-G

145658360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41888116-T-C

http://identifiers.org/hco/5/GRCh38#145658806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41888280-A-C

145658806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41888280-A-G

145658892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41888366-G-A

145658960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41888419-A-T

145659117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41888570-A-G

145659159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41888612-G-A

145659162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41888615-C-G

145659162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41888615-C-T

145659258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41888713-A-G

145659379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41888792-T-C

145659448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41888860-G-A

145659546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41888956-G-A

145659579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41888990-G-A

http://identifiers.org/hco/5/GRCh38#145659634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41889042-C-A

145659650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41889061-T-G

145659794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41889730-G-C

145659947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41889880-A-G

http://identifiers.org/hco/5/GRCh38#145660059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41889981-C-A

145660135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41890057-G-T

http://identifiers.org/hco/5/GRCh38#145660261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41890180-C-A

145660302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41890223-A-G

145660406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41890328-T-A

145660410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41890332-A-G

145660451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41890373-T-G

145660526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41890437-G-A

145660799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41890702-T-A

145661039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41891120-C-G

http://identifiers.org/hco/5/GRCh38#145661040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41891121-A-C

145661061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41891141-A-G

145661100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41891176-G-A

145661182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41891257-C-T

145661265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41891329-C-T

145661412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41891605-C-T

http://identifiers.org/hco/5/GRCh38#145661663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41891807-C-A

145661897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41893012-T-C

145661917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41893032-T-C

145662100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41893187-T-C

145662113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41893200-G-A

145662132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41893219-T-C

145662205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41893295-G-A

145662299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41893384-G-A

145662434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41893522-C-T

145662461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41893550-G-C

145663050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41893647-T-C

145663172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41893770-C-G

145663209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41893796-C-T

145663520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894105-G-A

145663540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894125-T-A

145663630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894390-T-C

http://identifiers.org/hco/5/GRCh38#145663710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41894459-C-A

145663715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894464-C-T

http://identifiers.org/hco/5/GRCh38#145663764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41894510-C-A

145663869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894610-C-T

145664189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894929-T-C

145664437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41895161-T-C

http://identifiers.org/hco/5/GRCh38#145664511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41895232-C-A

145664771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41895483-C-T

http://identifiers.org/hco/5/GRCh38#145665046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41895725-A-C

http://identifiers.org/hco/5/GRCh38#145665390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41896029-C-A

145665407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41896041-C-T

145665423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41896051-T-C

145665629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41896215-T-C

145665798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41896372-T-C

145665798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41896372-T-G

http://identifiers.org/hco/5/GRCh38#145665834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41896401-A-C

145665987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41896553-A-T

145666359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41896846-G-A

145666566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41897030-C-G

145666566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41897030-C-T

145666621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41897084-C-G

145666624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41897086-G-A

145666624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41897086-G-C

145666709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41897168-A-G

145666806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41897264-T-C

145666932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41897388-A-G

145666932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41897388-A-T

145666986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41897445-T-C

145667003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41897462-G-A

145667003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41897462-G-C

145667097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41897801-T-C

145667656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41898929-T-C

145667665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41898938-T-A

145667680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41898953-C-T

145668198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41899417-G-A

145668236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41899450-C-T

145668571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41899801-A-G

145668838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41900068-G-A

145668863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41900087-C-T

145668906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41900130-G-A

145668955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41900179-C-T

145669516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41900695-A-G

145669742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41900924-T-C

145670767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41901179-C-T

145671222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41901632-A-G

http://identifiers.org/hco/5/GRCh38#145671322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41901733-C-A

145671607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41901988-G-A

145671902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41902232-A-G

145671973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41902305-T-C

145672535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41902760-A-G

145672550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41902775-C-T

145676733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41913228-G-A

145676962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41913485-A-T

145677263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41913856-T-C

145677271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41913864-C-T

145677330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41913900-T-A

145677347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41913909-G-A

145677407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41913990-G-A

145677452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41914044-G-A

145677515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41914096-A-G

145677558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41914139-G-T

145677691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41914243-T-C

145677742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41914287-A-G

145677903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41917396-A-T

145679017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41915781-T-C

145679070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41915732-G-T

145679229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41915542-G-T

145679535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41915091-G-A

145679599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41915048-C-G

145679897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41914807-T-C

145679990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41914747-T-C

145680341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41914417-C-T

http://identifiers.org/hco/5/GRCh38#145680346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41914412-C-A

145680346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41914412-C-T

145680475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41917538-T-C

145680570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41917631-G-C

145680590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41917663-A-G

145680992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41918147-T-C

145681084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41918254-C-T

145681086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41918256-G-A

http://identifiers.org/hco/5/GRCh38#145681122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41918303-C-A

145681158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41918338-G-A

145681229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41918404-G-T

145681230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41918405-C-T

145681907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41919087-G-A

145681927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41919107-G-A

145682088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41919266-T-C

145682210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41919389-A-G

145682399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41919596-A-G

145682570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41919765-C-T

145682691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41919864-T-C

145682732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41919905-G-A

145682901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41920074-T-A

145682948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41920117-G-A

145683105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41920268-T-C

145683106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41920269-A-G

145683228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41920396-G-A

145683492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41920621-G-C

145683493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41920622-T-C

145683502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41920631-A-G

http://identifiers.org/hco/5/GRCh38#145683540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41920668-C-A

145683569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41920698-T-C

145683630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41920755-C-T

145683844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41927406-A-G

145683864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41927427-A-G

145683996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41927555-C-T

145684095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41927631-G-A

145684140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41927657-T-C

145684239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41927760-C-T

145684281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41927803-A-G

145684308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41927830-G-A

145684520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41927976-C-T

145684566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41928017-C-T

145684593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41928047-A-G

145684647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41929858-G-A

145684776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41929989-G-A

145684776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41929989-G-C

145685505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41930647-A-G

145685725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41930868-G-A

145685811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41930948-C-T

145686739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41933030-G-A

145686902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41933191-G-T

145687203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41933485-G-A

145687266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41933546-C-T

145687329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41933597-C-T

145687567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41933805-T-C

145687605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41933913-C-T

145687704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41934014-T-C

145688034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41934338-G-A

145688034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41934338-G-T

145688243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41934547-G-A

145688461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41934766-C-T

http://identifiers.org/hco/5/GRCh38#145688514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41935071-A-C

145688714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41935267-C-T

145688754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41935307-T-C

http://identifiers.org/hco/5/GRCh38#145688801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41935360-C-A

145688849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41935404-G-A

145690339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41938146-T-C

145690404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41938212-G-A

http://identifiers.org/hco/5/GRCh38#145690684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41938484-C-A

145690730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41938530-T-C

http://identifiers.org/hco/5/GRCh38#145691026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41938826-C-A

http://identifiers.org/hco/5/GRCh38#145691164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41938978-C-A

145691164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41938978-C-T

http://identifiers.org/hco/5/GRCh38#145691702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41939438-A-C

145691736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41939470-G-A

145691802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41939535-T-C

145691999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41939688-T-C

145692025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41939713-T-G

http://identifiers.org/hco/5/GRCh38#145692492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41940214-A-C

145692726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41940450-A-G

145694092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41941564-G-A

145694095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41941567-C-T

http://identifiers.org/hco/5/GRCh38#145694182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41941630-C-A

145694182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41941630-C-T

145694196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41941649-T-C

145694311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41941747-A-G

145694514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41941928-T-A

http://identifiers.org/hco/5/GRCh38#145694641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41942657-A-C

145694646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41942662-A-G

145694815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41942828-A-G

145696903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41944074-T-C

145696925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41944096-A-T

145697037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41944415-A-G

145697037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41944415-A-T

145697050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41944428-T-C

145697053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41944431-A-G

145697057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41944435-A-G

145697060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41944438-T-C

145697065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41944443-A-G

145697286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41944696-A-G

http://identifiers.org/hco/5/GRCh38#145697435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#41944851-A-C

145697585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41944984-A-G

145697638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41945040-A-G

145697638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41945040-A-T

145697641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41945043-G-C

145698495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41945944-T-G

145699193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41946289-T-C

http://identifiers.org/hco/5/GRCh38#145699546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41946586-C-A

145699819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41946812-C-T

http://identifiers.org/hco/5/GRCh38#145699820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41946813-A-C

145699820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41946813-A-G

145699845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41946838-G-C

145699845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41946838-G-T

145699906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41946902-C-T

145700210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41947181-A-G

http://identifiers.org/hco/5/GRCh38#145700621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41947614-A-C

145700887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41947811-A-T

145700891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41947815-G-A

145700891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41947815-G-T

145700961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41947889-G-A

145700983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41947908-C-G

145701113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41948019-G-A

145701113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41948019-G-T

145701272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41949366-C-T

145701375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41949467-T-C

145701537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41949629-C-G

145702356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41950878-T-C

145702484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41950983-T-C

http://identifiers.org/hco/5/GRCh38#145702534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41951033-A-C

145702815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951304-A-G

145702934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951404-T-C

145703278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951745-G-A

http://identifiers.org/hco/5/GRCh38#145703413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41951919-C-A

http://identifiers.org/hco/5/GRCh38#145703541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41952057-C-A

145703580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41952096-T-C

145703610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41952126-T-C

http://identifiers.org/hco/5/GRCh38#145703999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41952534-C-A

145704063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41952590-G-A

145704266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 41952795-G-T

145704274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41952803-C-G

145704277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41952805-T-C

http://identifiers.org/hco/5/GRCh38#145704282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#41952810-C-A

145704574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28306
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41953087-G-A