55547927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: 3 prime UTR variant
orthologous variants: 29170408-A-T

55548067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: 3 prime UTR variant
orthologous variants: 29170275-G-T

55548103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: 3 prime UTR variant
orthologous variants: 29170249-T-C

55548959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: 3 prime UTR variant
orthologous variants: 29169424-T-G

55549440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: 3 prime UTR variant
orthologous variants: 29168976-G-C

http://identifiers.org/hco/2/GRCh38#55549733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29168726-A-C

55549903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: 3 prime UTR variant
orthologous variants: 29168557-T-A

55549903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: 3 prime UTR variant
orthologous variants: 29168557-T-C

55549906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: 3 prime UTR variant
orthologous variants: 29168554-A-G

55550140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29168306-T-A

http://identifiers.org/hco/2/GRCh38#55550368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29168079-C-A

55550438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29168019-T-A

55550729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29167772-T-G

55550738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29167763-C-G

55550738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29167763-C-T

55550840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29167656-G-C

55550879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29167618-T-G

55550926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29167561-T-G

http://identifiers.org/hco/2/GRCh38#55550953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29167535-A-C

55550953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29167535-A-G

55551034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29167462-C-T

55558784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: synonymous variant
orthologous variants: 29163785-T-C

55562934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29163279-T-C

55563108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29163123-G-A

55563228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29162922-G-C

55563245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29162902-G-A

55563492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29162593-C-G

55563703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29162396-G-A

55564185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29161975-A-G

55564185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29161975-A-T

http://identifiers.org/hco/2/GRCh38#55564211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29161949-C-A

http://identifiers.org/hco/2/GRCh38#55564268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29161866-A-C

55564268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29161866-A-G

55564298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29161804-T-C

55564705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29161426-C-T

55565100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29161055-T-G

http://identifiers.org/hco/2/GRCh38#55565138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29161020-A-C

55565282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29160875-T-C

http://identifiers.org/hco/2/GRCh38#55566656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29160244-A-C

55568161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29159525-A-T

http://identifiers.org/hco/2/GRCh38#55568719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29159008-C-A

55570460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29158457-C-G

55570460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29158457-C-T

55572853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29156371-T-C

55572929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29156306-G-C

55572987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29156253-A-G

55573508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29155828-C-G

http://identifiers.org/hco/2/GRCh38#55573819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29155504-A-C

55577292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152929-A-G

55577292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152929-A-T

55577358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: splice acceptor variant
orthologous variants: 29152863-T-A

55577358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: splice acceptor variant
orthologous variants: 29152863-T-C

55577398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152831-T-C

55577767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152387-C-T

55577918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152263-T-C

55577927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152253-A-G

http://identifiers.org/hco/2/GRCh38#55578143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29152103-C-A

55578143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152103-C-T

55578166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152081-A-G

55578181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152066-T-A

55578181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152066-T-C

http://identifiers.org/hco/2/GRCh38#55578184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29152063-C-A

55578184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152063-C-T

55578186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152061-T-A

55578186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152061-T-C

http://identifiers.org/hco/2/GRCh38#55578209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29152042-A-C

55578209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152042-A-G

55578209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29152042-A-T

http://identifiers.org/hco/2/GRCh38#55578246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29152011-C-A

55578259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, missense_variant
orthologous variants: 29151998-A-G

55578259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, missense_variant
orthologous variants: 29151998-A-T

55578274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, missense_variant
orthologous variants: 29151983-A-G

55578414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29151857-T-A

http://identifiers.org/hco/2/GRCh38#55578432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29151840-C-A

55578433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29151839-T-C

55578435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29151837-G-A

55578435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29151837-G-C

55578435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29151837-G-T

55578599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29151638-T-C

55578616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29151621-T-A

55578764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29151353-T-C

55579033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29151134-T-A

55579120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29151067-T-C

http://identifiers.org/hco/2/GRCh38#55579663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29150820-A-C

55579663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29150820-A-T

55580153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29150420-G-A

55580594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29149893-A-G

55580744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29149572-G-A

55580800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29149516-G-A

55580954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29149390-C-T

55581497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29148993-C-G

55581497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29148993-C-T

55581532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29148958-G-C

55581549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29148940-C-T

55581579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: synonymous variant
orthologous variants: 29148910-C-G

55581723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29148782-A-T

55581784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29148726-G-A

55581784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29148726-G-T

http://identifiers.org/hco/2/GRCh38#55581809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29148708-A-C

55581809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29148708-A-T

http://identifiers.org/hco/2/GRCh38#55581813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29148704-A-C

55581813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29148704-A-T

55581839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29148678-T-C

55581881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29148648-G-A

55581881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29148648-G-C

http://identifiers.org/hco/2/GRCh38#55581929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29148613-A-C

http://identifiers.org/hco/2/GRCh38#55581937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29148605-C-A

55582034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29148549-G-A

55582034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29148549-G-T

55584999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29147258-A-G

http://identifiers.org/hco/2/GRCh38#55585030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29147228-A-C

55585097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: missense variant
orthologous variants: 29147161-G-C

55585157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: missense variant
orthologous variants: 29147101-T-C

http://identifiers.org/hco/2/GRCh38#55585171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29147087-A-C

55585179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29147079-A-G

55585206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29147056-C-G

55585222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29147040-A-G

55585222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29147040-A-T

55585253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29147009-A-G

55586242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29146625-C-G

55586242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29146625-C-T

http://identifiers.org/hco/2/GRCh38#55586500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29146407-C-A

55586767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29146142-T-G

55588988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29144538-T-A

55588988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29144538-T-C

55589132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29144402-A-G

55589132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29144402-A-T

55589362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29144196-A-G

55590562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29143497-A-T

55590612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29143458-T-C

55590631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29143440-T-C

55590671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29143398-A-G

http://identifiers.org/hco/2/GRCh38#55590972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#29142552-A-C

55591641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29142237-T-C

http://identifiers.org/hco/2/GRCh38#55591822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29142064-A-C

55592168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29141769-A-G

55592468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29141455-C-G

http://identifiers.org/hco/2/GRCh38#55592643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29141237-C-A

55592773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29141147-T-A

55592790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29141130-A-T

55592915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29140917-C-T

55593308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29140379-A-T

55593537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29140125-T-C

55593761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139900-C-G

55593761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139900-C-T

55593786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139874-C-T

55593893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139769-A-G

55593893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139769-A-T

55594227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139637-T-C

55594304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139589-A-G

55594304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139589-A-T

55594365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139519-T-A

55594414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139474-G-C

55594488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139430-T-G

55594527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139411-A-T

55594598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139343-T-A

55594612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139329-C-T

55594691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139258-T-C

55594810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139070-G-A

55594824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron variant
orthologous variants: 29139056-A-G

55598929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29138059-T-C

55598929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29138059-T-G

http://identifiers.org/hco/2/GRCh38#55599053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29137935-A-C

55599053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137935-A-T

http://identifiers.org/hco/2/GRCh38#55599091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29137899-A-C

55599091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137899-A-G

55599091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137899-A-T

55599147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137851-T-A

55599147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137851-T-C

55601876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137226-C-T

55603268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29134436-T-A

55603940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29132577-A-T

http://identifiers.org/hco/2/GRCh38#55603942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29132575-C-A

55603942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29132575-C-G

55603942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29132575-C-T

http://identifiers.org/hco/2/GRCh38#55603943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29132574-A-C

55603943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29132574-A-G

55603954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29132561-T-A

55604093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29132422-A-G

55604187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29132332-T-C

http://identifiers.org/hco/2/GRCh38#55604262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29132250-A-C

55610333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29128050-A-T

55610693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127843-G-A

http://identifiers.org/hco/2/GRCh38#55611495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29127525-A-C

55611514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127506-T-C

55611534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127490-G-C

http://identifiers.org/hco/2/GRCh38#55613138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29127106-A-C

55613156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127085-T-C

55613156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127085-T-G

55613179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127057-G-C

55613492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29126734-T-G

http://identifiers.org/hco/2/GRCh38#55613594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29126488-C-A

http://identifiers.org/hco/2/GRCh38#55613609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29126473-A-C

55613622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29126462-G-A

55613674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29126410-C-T

55614229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29125923-T-A

55614244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29125908-A-G

55614264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29125883-G-A

55614412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29125747-T-C

55614662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29125509-G-T

http://identifiers.org/hco/2/GRCh38#55614861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29125327-C-A

55614861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29125327-C-T

http://identifiers.org/hco/2/GRCh38#55615233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29124950-A-C

55615233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29124950-A-G

55615319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29124863-A-T

55615329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29124853-A-T

55615343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29124833-T-C

55615389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29124790-C-T

http://identifiers.org/hco/2/GRCh38#55615507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29124670-C-A

55615507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 29124670-C-T

55615554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29124628-T-C

55615925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29124598-G-A

55615986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29124539-T-G

55616492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29124077-A-G

http://identifiers.org/hco/2/GRCh38#55616600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29123980-C-A

55616600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29123980-C-T

http://identifiers.org/hco/2/GRCh38#55616759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29123855-A-C

55616759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29123855-A-G

55616759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29123855-A-T

55616777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29123837-G-T

55616814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29123789-G-A

55617070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29123518-G-A

55617070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29123518-G-T

55617076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29123512-G-C

http://identifiers.org/hco/2/GRCh38#55617516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29123076-C-A

55617516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29123076-C-G

http://identifiers.org/hco/2/GRCh38#55617535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29123057-C-A

55617535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29123057-C-T

55617676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122908-A-G

55617676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122908-A-T

http://identifiers.org/hco/2/GRCh38#55617776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29122816-C-A

55617776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122816-C-G

55617776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122816-C-T

55617870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122736-C-T

55617876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 29122735-A-G

http://identifiers.org/hco/2/GRCh38#55617885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#29122726-C-A

55617885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 29122726-C-T

55617923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 29122689-G-A

55617923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 29122689-G-C

55617923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 29122689-G-T

55617930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 29122683-G-A

55617969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122622-G-T

55617978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 29122614-T-C

55617981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29122611-G-T

55618131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122482-A-G

55618221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122407-A-G

55618268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122356-T-C

http://identifiers.org/hco/2/GRCh38#55618757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29122150-C-A

55618757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122150-C-G

http://identifiers.org/hco/2/GRCh38#55618783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29122138-C-A

55618783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122138-C-T

http://identifiers.org/hco/2/GRCh38#55618789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29122132-C-A

55618789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122132-C-T

55618809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122123-T-C

55618823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122109-C-G

55618823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29267
most severe consequence: non coding transcript exon variant
orthologous variants: 29122109-C-T