51584497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63075197-T-G

http://identifiers.org/hco/13/GRCh38#51584505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63075205-C-A

51584505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63075205-C-G

51584505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63075205-C-T

http://identifiers.org/hco/13/GRCh38#51584594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63075282-C-A

51584594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63075282-C-T

http://identifiers.org/hco/13/GRCh38#51584620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63075308-C-A

http://identifiers.org/hco/13/GRCh38#51584665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#63075350-C-A

51584665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63075350-C-T

51584959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63075578-T-G

http://identifiers.org/hco/13/GRCh38#51584975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#63075590-C-A

51584975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63075590-C-G

51585257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63075808-G-A

51585270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63075821-G-T

51586003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63076499-G-A

51586003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63076499-G-T

51586044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 63076540-A-G

51586070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 63076566-G-T

51586134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63076618-A-G

51586220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63076707-G-C

51586344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63076805-A-G

51586573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63076897-C-T

51586685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63077005-A-G

51586938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63077239-T-C

51586990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63077294-C-T

51587036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63077340-T-C

51587213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63077483-G-A

http://identifiers.org/hco/13/GRCh38#51587324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63077583-C-A

51587525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63077772-A-T

http://identifiers.org/hco/13/GRCh38#51587625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63077865-C-A

51587647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63077949-C-G

51587647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63077949-C-T

51587782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63078189-T-C

51587876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63078291-G-A

51587876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63078291-G-C

http://identifiers.org/hco/13/GRCh38#51588046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63078409-C-A

51588046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63078409-C-T

51588058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63078421-G-T

51588062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63078425-G-A

51588100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63078453-G-C

51588100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63078453-G-T

51588172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63078525-G-A

51588172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63078525-G-T

http://identifiers.org/hco/13/GRCh38#51588219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63078571-C-A

51588219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63078571-C-G

51588219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63078571-C-T

51588230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63078582-G-A

51588230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63078582-G-T

51588314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63079038-A-G

51588351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63079055-T-C

http://identifiers.org/hco/13/GRCh38#51588369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63079073-C-A

51588892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63079727-T-C

http://identifiers.org/hco/13/GRCh38#51589095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63080239-C-A

51589155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63080293-C-T

51589287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63080397-G-T

51589339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63080445-G-A

51589345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63080449-A-T

51589508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63080950-T-C

51589529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63080971-C-T

51589882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63081271-G-A

51590018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63081381-G-A

51590437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63081867-A-G

51590561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63082122-G-A

http://identifiers.org/hco/13/GRCh38#51590651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63082232-C-A

http://identifiers.org/hco/13/GRCh38#51590773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63082326-C-A

51590903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63082456-T-A

51590906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63082459-G-T

51590931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63082483-G-T

51591089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63082621-G-T

51591114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63082648-G-A

51591114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63082648-G-T

http://identifiers.org/hco/13/GRCh38#51591191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#63082713-C-A

51591238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63082762-G-T

http://identifiers.org/hco/13/GRCh38#51591284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#63082808-C-A

51591284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63082808-C-T

51591285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63082809-G-T

51591307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63082829-T-A

51591646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63083216-C-T

http://identifiers.org/hco/13/GRCh38#51591693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63083263-C-A

51591896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63083703-G-T

http://identifiers.org/hco/13/GRCh38#51591905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63083712-C-A

51614635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63090483-C-T

51614865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63090675-A-T

51614953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63090766-C-T

51615079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63090891-A-G

51615153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63090977-A-G

51615407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63091194-T-A

51615475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63091246-A-G

51615489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63091259-C-T

51615491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63091261-G-A

51615639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63091371-G-A

51615906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63092004-A-G

51615925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63092023-C-G

51617677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63093001-A-G

51617728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63093053-T-G

51617773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63093095-G-A

51617773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63093095-G-T

51617812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63093136-T-A

51617812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63093136-T-C

51618353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63093656-T-C

51618357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63093660-C-T

51618672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63094401-C-T

51618750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63094464-T-C

http://identifiers.org/hco/13/GRCh38#51618766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63094479-C-A

51618767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63094480-T-C

51619142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63094778-C-T

51620912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63096118-T-G

51621365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63097240-C-T

51621374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63097249-G-A

51621498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63097360-T-G

51621723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63097590-T-C

51622087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63100132-A-G

51622129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63100174-A-G

51622149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63100195-A-G

51622149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63100195-A-T

51622332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63100358-A-T

51622345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63100371-A-G

51626211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63100745-A-G

51626239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63100773-T-G

http://identifiers.org/hco/13/GRCh38#51626361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63100975-A-C

51626390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63101009-A-G

51626479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63101083-T-C

51629153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63101955-T-A

51629195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63101997-A-G

http://identifiers.org/hco/13/GRCh38#51629572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63102916-C-A

http://identifiers.org/hco/13/GRCh38#51629610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63102954-A-C

51632603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63105428-T-C

51632652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63105484-A-G

51633279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63105981-G-A

51633282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63105984-C-G

51633505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63106198-G-C

51633625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63106288-G-C

51633855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63106387-T-C

51634119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63106577-A-G

51634119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63106577-A-T

51635378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63107737-C-G

51635378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63107737-C-T

51635471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63107795-T-C

51635473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63107797-G-A

51635569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63107877-G-C

51636930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63110002-C-T

51638338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63111604-C-T

51638361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63111623-T-G

51638393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63111656-C-T

51638404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63111667-A-G

51638494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63111755-A-G

51638497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63111758-C-G

51638497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63111758-C-T

http://identifiers.org/hco/13/GRCh38#51638969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63112212-A-C

51639343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63112563-G-A

51639374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63112717-C-T

51639410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63112829-C-G

51639410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63112829-C-T

51639766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63113579-G-T

51640119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63113920-A-G

51640214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63114018-C-T

51640215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63114019-T-A

51640215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63114019-T-C

51643054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63115215-G-C

51643452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63115659-C-T

http://identifiers.org/hco/13/GRCh38#51643462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63115669-C-A

51643507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63115711-A-G

http://identifiers.org/hco/13/GRCh38#51643763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63115907-C-A

51643763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63115907-C-T

51643817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63115960-A-G

51644031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63116183-G-T

51644067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63116219-G-A

51644078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63116239-G-A

51644287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63116709-C-G

51644310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63116732-C-T

51644965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63117339-G-A

51645071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63117426-A-G

51645179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63117542-A-G

51645557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63117911-C-G

51645629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63117980-T-G

51645713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63118035-T-G

51645980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63118247-G-A

51646006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63118271-C-T

51654631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63120346-T-A

51654672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63120407-T-G

51657635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63121152-T-G

51657837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63121352-A-G

51658104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63121547-A-G

51660920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63123588-G-A

51660948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63123614-G-A

51660948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63123614-G-C

http://identifiers.org/hco/13/GRCh38#51661064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63123735-A-C

51661077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63123748-C-T

51661081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63123752-C-T

51661083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63123754-G-C

51661146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63123815-G-C

51661151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63123819-T-A

51661160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63123828-A-T

51661278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63124063-C-G

51661487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63124594-A-T

51661490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63124597-T-C

51663490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63129978-G-A

51663495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63129983-A-G

51663632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63130033-G-A

51663650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63130040-C-T

51663898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63130234-A-G

51664022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63130318-C-T

51664279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63130567-G-C

51664708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63130949-C-T

51664920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63131157-G-A

51665460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63132679-T-C

51665633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63132827-T-C

51666038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63133205-A-G

51666038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63133205-A-T

51674708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63137268-G-A

51674974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63137515-A-G

51675064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63137601-G-T

51675130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63137665-A-G

51675575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63138121-G-A

51676293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63139036-G-A

51676483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63139199-T-C

51676609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63139303-A-G

51676800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63139511-G-C

51676906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63139828-C-T

51677074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63139979-A-T

51677190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63140101-T-C

51677297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63140624-G-T

51677319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63140645-G-T

51677512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63140829-A-G

51678196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63141373-A-T

51678286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63141455-T-C

51680565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63143378-G-A

51680582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63143395-G-T

51680711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63143502-G-T

51680740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63143531-C-T

51680763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63143554-C-G

51680837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63143625-C-T

http://identifiers.org/hco/13/GRCh38#51680838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63143626-C-A

51680865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63143655-C-G

51681232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63144026-C-T

51681256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63144043-C-T

51681324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63144091-T-C

51681390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63144155-G-A

51681560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63144540-C-G

51681929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63144850-C-T

51682026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63144947-C-T

51682177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63145318-A-G

51682186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63145327-C-T

51682326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63145457-C-T

51682467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147039-A-G

51682509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147091-T-C

51682951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147491-C-G

51682951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147491-C-T

51683061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147887-C-T

51683103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147927-G-A

51683141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147960-A-T

51683164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147982-C-T

51683340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63148308-T-A

51683358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63148363-T-C

51683504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63148534-G-C

51684107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63149018-A-G

51684311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63149269-A-G

http://identifiers.org/hco/13/GRCh38#51684438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63149410-C-A

51684763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63149720-C-T

51685059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63149992-G-A

51686486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63150297-T-G

51686896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63150855-C-G

51688932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63151947-A-G

51689001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63152009-C-T

51689034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63152030-G-T

51689099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63152101-C-T

51689195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63152169-G-A

51689276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63152231-G-C

51689516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63152783-G-A

51689531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63152798-T-C

51689531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63152798-T-G

51689828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63153034-T-A

51689828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63153034-T-C

51689892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63153089-T-C

51690167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63153318-C-T

51701153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63160749-T-C

51701552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63160848-G-A

51701552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63160848-G-T

51701665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63160961-G-A

51701749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63161044-T-G

51702462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63161344-G-A

51702491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63161373-T-G

51702561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63161422-C-G

51702564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63161425-C-T

51702666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63161530-C-T

51703225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162021-G-T

51703236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162034-A-G

51703277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162073-G-A

51703573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162556-A-G

51703573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162556-A-T

51703576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162559-A-G

51703576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162559-A-T

51703683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162662-G-A

51703683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162662-G-C

51703683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162662-G-T

51703712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162691-C-T

http://identifiers.org/hco/13/GRCh38#51703732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63162710-C-A

51703732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162710-C-T

51703928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162872-C-T

51703940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162884-T-C

http://identifiers.org/hco/13/GRCh38#51704053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63163001-A-C

51704635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63163506-G-A

51704882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163660-C-G

51705045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163805-G-A

51706321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63164838-A-G

51718148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63166010-G-A

51718278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63166098-G-A

51718798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167106-T-A

51718798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167106-T-C

http://identifiers.org/hco/13/GRCh38#51719070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63167315-C-A

51719070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167315-C-G

51719101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167344-G-A

51719101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167344-G-T

51719124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167373-C-T

51719135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167477-G-A

51719135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167477-G-C

51719135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167477-G-T

http://identifiers.org/hco/13/GRCh38#51719359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63167838-C-A

51719359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167838-C-G

51719359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167838-C-T

51719413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167870-A-G

http://identifiers.org/hco/13/GRCh38#51719459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63167926-C-A

51719459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167926-C-T

51719534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63168002-G-A

51719701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63168156-A-G

51719740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63168200-C-T

51719877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63168510-C-T

51719889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63168522-A-G

51719913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63168550-C-T

51719991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63168623-G-A

51720274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63168873-A-G

51720409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63168993-G-T

51720410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63168994-C-T

51721571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63169359-G-T

51721820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63169603-G-A

http://identifiers.org/hco/13/GRCh38#51721982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63169759-C-A

51721982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63169759-C-T

51722282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63170012-C-T

51722451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63170123-G-A

51722643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63170251-A-G

51722656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63170264-C-T

http://identifiers.org/hco/13/GRCh38#51722877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63170474-C-A

51722877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63170474-C-T

51722878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63170475-G-A

http://identifiers.org/hco/13/GRCh38#51727558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63171627-C-A

51727811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63171873-G-A

http://identifiers.org/hco/13/GRCh38#51727842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63171904-C-A

51727844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63171906-G-A

http://identifiers.org/hco/13/GRCh38#51727894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63171945-C-A

51727939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63171996-A-G

51727939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63171996-A-T

51727941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63171998-G-A

51727941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63171998-G-T

51728106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172134-A-G

51728342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172312-A-G

51728345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172315-G-C

51728409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172377-T-A

51728421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172389-T-G

51728488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172469-G-A

51728582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172565-T-C

51728589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172571-A-G

51728605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172587-G-A

51729041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172755-C-T

51729256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172951-G-A

51729276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63172971-C-T

51729347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63173038-T-C

51729361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63173042-C-T

51729692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63173198-A-G

51729710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63173216-G-A

51729841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63173313-T-G

51729843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63173315-A-T

51730145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63173541-T-C

51730478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63173871-T-C

51730482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63173875-C-T

51730483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63173876-C-T

51730541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63173932-C-T

51730546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63173937-C-G

http://identifiers.org/hco/13/GRCh38#51730907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63174233-A-C

51730979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63174302-T-A

http://identifiers.org/hco/13/GRCh38#51731153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63174577-A-C

51731174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63174599-C-G

51731406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63174769-T-C

51731651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63174952-G-A

51731737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63175040-G-A

51731810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63175097-A-G

51731810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63175097-A-T

51732209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63175582-C-T

51732358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63175662-G-C

51732372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63175677-G-A

51732940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63176141-G-A

51734124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63176633-G-A

51734126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63176635-T-A

http://identifiers.org/hco/13/GRCh38#51734155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63176663-C-A

51737035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63177811-C-T

51737038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63177814-G-C

51737088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63177857-C-G

http://identifiers.org/hco/13/GRCh38#51737103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63177872-A-C

51737190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63177938-A-T

51737427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178061-C-T

51737510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178135-T-C

51737510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178135-T-G

51737605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178199-T-A

51737605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178199-T-C

51737605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178199-T-G

51737614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178208-G-A

51737666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178250-G-A

51737686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178267-C-T

51737698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178278-C-T

51737798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178332-C-T

51737835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178356-C-T

51737836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178357-A-G

51737869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178384-A-G

51737882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178397-T-C

51738110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178565-A-G

http://identifiers.org/hco/13/GRCh38#51738900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63181332-C-A

51738900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181332-C-G

51738900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181332-C-T

51739000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181421-G-A

51739011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 63181432-A-G

51739031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63181452-T-C

51739039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63181460-G-A

51739039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63181460-G-T

51739087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63181508-G-A

51739188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181609-G-A

51739188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181609-G-T

51739204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181627-T-C

51739204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181627-T-G

51739287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181705-G-T

http://identifiers.org/hco/13/GRCh38#51739289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63181707-C-A

51739289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181707-C-T

51739507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181906-G-T

51744822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63182843-A-G

51744871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63182858-C-T

http://identifiers.org/hco/13/GRCh38#51745016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63182965-A-C

51751048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63185871-C-G

51751227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63186012-T-C

51751233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63186017-G-T

51751481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63186237-C-G

51751921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63186416-A-G

51752381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63186838-A-G

51752541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63186966-A-T

51752714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63187080-A-G

51752932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63187245-T-C

51753044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63187344-A-G

51753067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63187367-G-C

51753170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63187435-C-G

51753170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63187435-C-T

51753217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63187482-A-G

51755161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63189196-T-C

http://identifiers.org/hco/13/GRCh38#51755287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63189300-C-A

51755298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63189311-G-A

http://identifiers.org/hco/13/GRCh38#51755306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63189318-C-A

51755306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63189318-C-T

51755381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63189387-T-C

http://identifiers.org/hco/13/GRCh38#51755491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63189492-A-C

51755542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63189545-G-T

51755860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63189817-A-G

51756297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63190428-C-T

51756301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63190432-G-C

51756307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63190438-T-C

http://identifiers.org/hco/13/GRCh38#51756308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63190439-A-C

51756308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63190439-A-G

51756358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63190487-C-T

51756642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63190731-G-C

51756664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63190753-A-G

51756860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63190934-C-T

51756876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63190950-G-A

51757186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63191180-T-C

51757523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63191469-G-A

51757590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63191526-T-G

51757637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63191573-A-T

51757757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63191753-A-G

51757860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63191830-T-C

51757862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63191832-C-T

http://identifiers.org/hco/13/GRCh38#51758049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63192191-A-C

51758049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63192191-A-G

http://identifiers.org/hco/13/GRCh38#51758163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63192289-C-A

51758163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63192289-C-T

http://identifiers.org/hco/13/GRCh38#51758167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63192293-C-A

51758167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63192293-C-G

51758181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63192299-G-A

51758181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63192299-G-T

51758194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63192312-G-A

51758194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63192312-G-T

51758294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 63192412-T-C

51758361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63192474-A-G

51759618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63193590-A-G

51759618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63193590-A-T

51759794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63193782-T-C

http://identifiers.org/hco/13/GRCh38#51759826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63193809-C-A

51759832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63193816-A-G

51759832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63193816-A-T

http://identifiers.org/hco/13/GRCh38#51759876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63193861-C-A

51759876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63193861-C-T

51759878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63193863-A-G

51759928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63193907-G-A

51759928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63193907-G-T

http://identifiers.org/hco/13/GRCh38#51760017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63193998-C-A

51760017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63193998-C-T

51760034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63194019-G-T

http://identifiers.org/hco/13/GRCh38#51760128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63194114-C-A

51760205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63194185-C-G

51760232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63194214-T-A

51760232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63194214-T-C

51760452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63194392-T-A

51761155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63194795-T-C

51761393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63194929-A-G

51761423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63194960-G-A

51761423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63194960-G-T

51761546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63195078-G-T

51761706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63195229-T-C

51761706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63195229-T-G

http://identifiers.org/hco/13/GRCh38#51761942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63195416-C-A

51761942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63195416-C-T

51761969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63195442-G-T

51762243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63195688-G-A

http://identifiers.org/hco/13/GRCh38#51762308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63195724-C-A

51762308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63195724-C-T

51762582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63195976-A-G

51762583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63195977-G-T

http://identifiers.org/hco/13/GRCh38#51762718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63196095-C-A

51762718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63196095-C-G

51762756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63196130-A-G

51762756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63196130-A-T

51762769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63196139-G-T

http://identifiers.org/hco/13/GRCh38#51763015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63196367-C-A

51763107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63196450-G-A

http://identifiers.org/hco/13/GRCh38#51763150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63196493-A-C

51763890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63196911-G-A

http://identifiers.org/hco/13/GRCh38#51763983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63197009-C-A

51764116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63197133-G-A

51764116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63197133-G-T

51765997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63198125-G-T

51766010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63198154-G-T

http://identifiers.org/hco/13/GRCh38#51766091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63198221-C-A

51766091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63198221-C-T

51766120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63198250-G-A

51766358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63198470-C-T

http://identifiers.org/hco/13/GRCh38#51766504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63198645-C-A

51766504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63198645-C-T

51766509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63198650-G-A

51766509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63198650-G-T

51766559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63198725-T-C

51766622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63198788-A-G

http://identifiers.org/hco/13/GRCh38#51766799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63198957-A-C

51766799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63198957-A-G

51766911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199071-T-A

51766911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199071-T-C

51767036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199181-A-T

51767087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199233-G-T

51767143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199316-A-G

51767156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199328-G-A

51767171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199342-G-T

51767181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199352-C-T

51767209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199374-G-T

51767255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199430-G-T

51767477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199611-A-G

51767477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199611-A-T

51767493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199626-G-A

51767493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199626-G-T

51767513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199646-C-G

51767513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63199646-C-T

http://identifiers.org/hco/13/GRCh38#51767569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20482
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#63199698-C-A