61873697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10035414-G-T

61873888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10035236-G-A

61873888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10035236-G-T

61873902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10035222-G-T

http://identifiers.org/hco/11/GRCh38#61873961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10035150-C-A

61873961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10035150-C-T

http://identifiers.org/hco/11/GRCh38#61873964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10035147-C-A

61873965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10035146-A-G

61873965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10035146-A-T

61873971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10035140-T-C

61873971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10035140-T-G

61873972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10035139-G-T

61874453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10034864-G-A

61874515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10034817-T-A

http://identifiers.org/hco/11/GRCh38#61874549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10034782-C-A

61874549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10034782-C-T

61874633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10034700-C-G

61874633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10034700-C-T

61874684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10034663-C-T

61874701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10034645-G-A

61874802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10034540-C-T

61875678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10034087-G-A

61875749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10034043-G-T

61875772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10033998-G-A

61875772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10033998-G-T

61875807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10033963-C-G

61875809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10033961-T-C

http://identifiers.org/hco/11/GRCh38#61875818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10033953-C-A

61875818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10033953-C-T

61875839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10033924-C-G

http://identifiers.org/hco/11/GRCh38#61875902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10033861-C-A

61875902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10033861-C-T

http://identifiers.org/hco/11/GRCh38#61875917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10033846-A-C

http://identifiers.org/hco/11/GRCh38#61876075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10033707-C-A

61876239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10033530-G-T

61876325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10033473-C-G

61876325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10033473-C-T

61876470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10033337-G-A

http://identifiers.org/hco/11/GRCh38#61876475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10033332-C-A

61876614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10033285-G-A

61876614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10033285-G-T

http://identifiers.org/hco/11/GRCh38#61876666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10033270-C-A

61876666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10033270-C-T

http://identifiers.org/hco/11/GRCh38#61876668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10033268-A-C

http://identifiers.org/hco/11/GRCh38#61876677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10033259-C-A

61876677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10033259-C-T

http://identifiers.org/hco/11/GRCh38#61876717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10033219-C-A

61876717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10033219-C-T

61876738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10033195-T-C

61876783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10033152-G-T

61876794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10033142-G-T

61876818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10033119-T-C

61876830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10033107-G-A

http://identifiers.org/hco/11/GRCh38#61876856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10033081-C-A

61876856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10033081-C-G

61876926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10032996-A-G

61877024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032908-T-A

61877024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032908-T-C

http://identifiers.org/hco/11/GRCh38#61877043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10032889-C-A

61877043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032889-C-T

http://identifiers.org/hco/11/GRCh38#61877083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10032857-C-A

http://identifiers.org/hco/11/GRCh38#61877096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10032855-C-A

61877198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032750-G-A

61877198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032750-G-C

http://identifiers.org/hco/11/GRCh38#61877206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10032742-C-A

61877206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032742-C-G

61877206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032742-C-T

http://identifiers.org/hco/11/GRCh38#61877267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10032690-C-A

61877267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032690-C-G

61877267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032690-C-T

http://identifiers.org/hco/11/GRCh38#61877272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10032685-A-C

61877272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032685-A-G

61877349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032669-G-T

http://identifiers.org/hco/11/GRCh38#61877397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10032654-A-C

61877397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032654-A-G

61877446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032605-T-C

61877483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032574-G-A

61877483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032574-G-T

61877717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032355-G-A

61877717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032355-G-C

61877717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032355-G-T

61877747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032325-A-G

61877747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032325-A-T

http://identifiers.org/hco/11/GRCh38#61877754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10032316-C-A

61877754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032316-C-T

61877760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032310-T-C

61877820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032227-T-C

61878106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10032076-G-T

http://identifiers.org/hco/11/GRCh38#61878445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10031779-C-A

61878445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10031779-C-G

http://identifiers.org/hco/11/GRCh38#61878500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10031723-C-A

http://identifiers.org/hco/11/GRCh38#61878673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10031546-C-A

61878673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10031546-C-T

http://identifiers.org/hco/11/GRCh38#61878732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10031497-C-A

61878864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10031365-G-A

61878864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10031365-G-T

http://identifiers.org/hco/11/GRCh38#61878946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10031311-C-A

61878946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10031311-C-G

61878950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10031307-T-C

61879253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10030427-G-A

61879253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10030427-G-T

61879272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10030407-T-C

61879273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10030406-T-A

61879273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10030406-T-C

61879273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10030406-T-G

61879328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10030379-A-G

61879496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10030211-T-C

http://identifiers.org/hco/11/GRCh38#61879659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10030047-C-A

61879659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10030047-C-T

http://identifiers.org/hco/11/GRCh38#61879889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10029788-C-A

61879889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10029788-C-T

http://identifiers.org/hco/11/GRCh38#61879927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10029751-C-A

61879927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10029751-C-G

61879927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10029751-C-T

61880111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10029604-C-T

61880144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10029571-A-G

http://identifiers.org/hco/11/GRCh38#61880235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10029487-A-C

61880245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10029481-G-A

61880245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10029481-G-T

61880256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10029470-A-G

61880322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028940-C-T

61880358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028903-C-T

http://identifiers.org/hco/11/GRCh38#61880378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10028883-C-A

61880572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028719-T-C

61880773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028524-A-T

61880784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028514-C-G

61880784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028514-C-T

http://identifiers.org/hco/11/GRCh38#61880910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10028472-C-A

61880913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028469-G-A

61881055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028382-T-C

61881057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028380-A-T

http://identifiers.org/hco/11/GRCh38#61881070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10028377-A-C

61881080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028367-G-A

61881080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028367-G-T

61881099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028348-G-C

61881099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028348-G-T

61881238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028200-T-C

61881248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028190-G-A

61881248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028190-G-C

61881248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028190-G-T

61881256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028182-G-T

61881259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028178-T-A

61881269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028168-G-A

61881269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028168-G-C

61881269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028168-G-T

61881271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028166-G-A

61881271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028166-G-T

61881273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028164-G-A

61881273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028164-G-T

61881277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028160-A-G

61881277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028160-A-T

http://identifiers.org/hco/11/GRCh38#61881285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10028152-C-A

61881285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028152-C-T

61881287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028150-G-C

61881287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028150-G-T

61881319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10028117-A-G

61881555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10027913-A-G

61881652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10027820-G-A

61881816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10027227-C-G

61881816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10027227-C-T

61881927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10027117-G-A

61881928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10027116-G-T

61881980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10027076-G-C

61883409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10026330-T-C

61883422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10026295-C-T

http://identifiers.org/hco/11/GRCh38#61883452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10026265-C-A

61883963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10025973-C-T

http://identifiers.org/hco/11/GRCh38#61885041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10025073-C-A

61885316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10024820-C-G

61885537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10024614-A-G

61885571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10024581-C-T

61885778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10024381-C-T

61885791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10024368-T-C

61886082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10024081-C-T

http://identifiers.org/hco/11/GRCh38#61886340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10023785-C-A

61886340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10023785-C-T

http://identifiers.org/hco/11/GRCh38#61886410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10023706-C-A

61886410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10023706-C-T

61886514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10023449-G-C

61886517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10023439-G-A

61886517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10023439-G-C

http://identifiers.org/hco/11/GRCh38#61886614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10023341-C-A

61886648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10023307-C-G

61886648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10023307-C-T

61887557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10021810-C-T

61887651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10021724-C-G

61887652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10021723-T-C

61888451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10021002-T-C

61888667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10020813-C-T

61888872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10020639-C-G

61888872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10020639-C-T

http://identifiers.org/hco/11/GRCh38#61890382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10020119-C-A

61890382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10020119-C-T

http://identifiers.org/hco/11/GRCh38#61890491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10020011-C-A

61890491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10020011-C-T

61890663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10019845-G-T

http://identifiers.org/hco/11/GRCh38#61890770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#10019720-A-C

61890954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10019534-G-A

http://identifiers.org/hco/11/GRCh38#61891061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#10019435-C-A

61891061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10019435-C-G

61891061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10019435-C-T

61891371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10019104-A-G

61891385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 10019086-G-A

61891385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 10019086-G-T

61891399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 10019074-T-A

61891399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 10019074-T-C

61891519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 10018960-T-A

61891519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 10018960-T-C

http://identifiers.org/hco/11/GRCh38#61891635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10018862-C-A

http://identifiers.org/hco/11/GRCh38#61891636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10018861-C-A

61891636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron variant
orthologous variants: 10018861-C-T

http://identifiers.org/hco/11/GRCh38#61891724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10018773-C-A

61891724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron variant
orthologous variants: 10018773-C-T

http://identifiers.org/hco/11/GRCh38#61891775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10018718-C-A

61891775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron variant
orthologous variants: 10018718-C-T

http://identifiers.org/hco/11/GRCh38#61891815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#10018687-C-A

61891815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, undefined
orthologous variants: 10018687-C-G

61891815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron_variant, undefined
orthologous variants: 10018687-C-T

61891844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron variant
orthologous variants: 10018658-G-A

61891844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron variant
orthologous variants: 10018658-G-C

61891844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: intron variant
orthologous variants: 10018658-G-T

http://identifiers.org/hco/11/GRCh38#61891870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#10018637-C-A

61891875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 10018625-A-G

61891905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 10018595-G-T

61891957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 10018531-C-T

61891992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3576
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 10018503-A-G