182890246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48594573-A-T

182890276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48594546-G-T

182890309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48594513-G-A

182890315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48594507-G-A

http://identifiers.org/hco/4/GRCh38#182890336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48594488-C-A

182890348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48594472-A-G

182890365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48594455-G-T

182890369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48594451-G-A

182890369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48594451-G-T

http://identifiers.org/hco/4/GRCh38#182890548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48594284-C-A

182890587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48594234-A-T

http://identifiers.org/hco/4/GRCh38#182891029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48593822-C-A

182891070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48593781-A-G

182891128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48593742-G-A

182891128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48593742-G-T

http://identifiers.org/hco/4/GRCh38#182891129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48593741-A-C

182891129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48593741-A-G

http://identifiers.org/hco/4/GRCh38#182891200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48593679-C-A

182891200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48593679-C-G

182891200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48593679-C-T

http://identifiers.org/hco/4/GRCh38#182891203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48593676-A-C

182891203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48593676-A-G

182891203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48593676-A-T

182891271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48593618-T-C

182891301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48593595-G-A

182891337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48593559-G-T

182891455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48593398-T-C

http://identifiers.org/hco/4/GRCh38#182891491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48593361-C-A

182891491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48593361-C-G

182891491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48593361-C-T

182891540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48593303-G-A

182891540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48593303-G-T

182891881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48592966-T-C

182892057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48592824-A-G

182892672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48592243-C-T

182892685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48592230-T-C

182892734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48592180-T-A

http://identifiers.org/hco/4/GRCh38#182892904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48592019-C-A

http://identifiers.org/hco/4/GRCh38#182892928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48591995-C-A

182892928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48591995-C-T

182892969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48591943-A-G

182893073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48591869-G-A

182893091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48591851-T-C

182893206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48591749-C-G

182893206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48591749-C-T

http://identifiers.org/hco/4/GRCh38#182893276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48591683-A-C

182893281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48591678-C-T

182893319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48591642-C-T

182893510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48591444-G-A

182893601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48591358-C-T

http://identifiers.org/hco/4/GRCh38#182893641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48591319-C-A

182893673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48591279-C-G

182893673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48591279-C-T

182894148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48590779-G-C

182894356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48590568-A-G

182894374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48590550-A-G

182894374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48590550-A-T

182894387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48590537-T-C

http://identifiers.org/hco/4/GRCh38#182894420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48590503-C-A

182894420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48590503-C-T

http://identifiers.org/hco/4/GRCh38#182894477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48590419-C-A

182894724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48590188-A-G

182894738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48590174-G-A

182895050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48589852-A-G

http://identifiers.org/hco/4/GRCh38#182896611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48587847-C-A

182896659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48587807-G-A

182896700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48587771-G-A

http://identifiers.org/hco/4/GRCh38#182896721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48587750-C-A

182896721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48587750-C-T

182896844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48587624-G-A

182896979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48587458-G-C

182897034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48587399-T-C

182897034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48587399-T-G

182897238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48587205-T-G

182897422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48587544-G-A

182898035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48586294-G-A

182898291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48586070-G-A

182898307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48586054-C-T

182898314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48586048-A-T

182898380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48585982-G-A

182898387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48585979-C-T

182900695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48584619-T-C

http://identifiers.org/hco/4/GRCh38#182900798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48584521-C-A

182900800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48584519-T-C

182900861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48584463-T-G

http://identifiers.org/hco/4/GRCh38#182900904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48584421-C-A

182900904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48584421-C-T

182901183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48584126-A-G

182901941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48583738-C-T

182902347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48582753-T-C

182902371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48582727-C-T

http://identifiers.org/hco/4/GRCh38#182902489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48582586-C-A

182902539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48582498-G-A

182902688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48582361-G-A

182902690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48582359-T-C

182902762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48582293-G-A

182902966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48582136-A-T

http://identifiers.org/hco/4/GRCh38#182903002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48582101-C-A

182903228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48581860-C-T

182903348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48581769-C-T

182903440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48581692-G-A

182903461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48581672-T-A

http://identifiers.org/hco/4/GRCh38#182903725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48581260-A-C

182903910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48580993-G-A

182903910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48580993-G-C

182904070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48580818-C-T

182904565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48580279-A-G

182904571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48580273-C-T

182904668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48580173-T-C

182904702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48580138-C-T

182904786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48580068-T-C

182904801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48580053-C-T

182904927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48579981-C-G

http://identifiers.org/hco/4/GRCh38#182905075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48579867-C-A

182905115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48579832-C-T

182905139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48579811-T-C

182906635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48578900-T-C

182906688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48578849-G-A

http://identifiers.org/hco/4/GRCh38#182906742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48578796-A-C

182906823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48578715-G-C

182906902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48578632-C-T

182906936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48578620-C-T

182907010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48578552-G-A

182907066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48578516-T-C

182907069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48578513-C-T

182907070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48578512-T-G

182907503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48578388-G-A

182907699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48578067-G-A

182907932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48577413-G-A

182908021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48577329-T-C

182909280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48575591-T-C

182909671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48575251-C-T

182909838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48575085-G-A

182909919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48575001-G-A

182909974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48574947-G-A

http://identifiers.org/hco/4/GRCh38#182910014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48574804-C-A

182910085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48574727-G-A

182910085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48574727-G-C

182910173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48574645-G-C

182910239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48574578-G-A

182910239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48574578-G-C

182910959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48573786-A-G

182911167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48573595-T-C

182911167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48573595-T-G

182912137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48569877-T-A

182912578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48569450-G-A

182912730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48569311-G-T

182912917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48568696-G-A

http://identifiers.org/hco/4/GRCh38#182913385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48568230-C-A

182913621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48567573-C-T

182913639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48567552-C-T

182914034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48567122-G-A

182914034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48567122-G-C

182914111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48567056-G-A

182914151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48567017-G-A

http://identifiers.org/hco/4/GRCh38#182914778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48565768-C-A

182914778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48565768-C-G

182914778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48565768-C-T

182914819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48565218-G-T

http://identifiers.org/hco/4/GRCh38#182914830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48565209-C-A

http://identifiers.org/hco/4/GRCh38#182915105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48564962-C-A

182915105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48564962-C-G

http://identifiers.org/hco/4/GRCh38#182915179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48564938-C-A

182915179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48564938-C-T

182915416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48564864-C-T

182915586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48564698-A-T

182915687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48564615-A-T

182915756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48564537-A-T

182915846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48564247-T-C

182915863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48564231-A-G

182915863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48564231-A-T

182915917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48564188-G-A

182915917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48564188-G-T

182915952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48564161-G-C

182915952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48564161-G-T

182915957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48564156-C-T

182916179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48563895-C-G

182916316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48563814-G-A

182916316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48563814-G-C

182916376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48563777-A-G

182916386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48563767-G-A

182916386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48563767-G-T

182916650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48563688-G-A

182916658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48563680-A-G

http://identifiers.org/hco/4/GRCh38#182916669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48563670-C-A

182916669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48563670-C-T

182916761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48563641-G-A

182916761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48563641-G-T

182916777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 48563628-G-A

182916777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48563628-G-T

182916786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 48563619-T-A

182916786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 48563619-T-C

182916920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48563471-G-A

182916920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48563471-G-T

http://identifiers.org/hco/4/GRCh38#182916951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48563459-C-A

182916951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48563459-C-T

http://identifiers.org/hco/4/GRCh38#182916958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48563452-C-A

http://identifiers.org/hco/4/GRCh38#182917039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48563379-A-C

182917039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48563379-A-G

182917084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48563355-C-T

182917194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 48563303-G-A

182917287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_donor_variant, undefined
orthologous variants: 48563253-C-T

182917450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 48563129-G-A

http://identifiers.org/hco/4/GRCh38#182917458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48563121-C-A

182917458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 48563121-C-T

182917510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 48563054-T-G

182917538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 48563028-T-A

182917538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 48563028-T-C

182917538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 48563028-T-G

http://identifiers.org/hco/4/GRCh38#182917542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48563024-C-A

182917542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 48563024-C-T

http://identifiers.org/hco/4/GRCh38#182917762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#48562873-C-A

182917762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: intron_variant, undefined
orthologous variants: 48562873-C-T

182917882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5 prime UTR variant
orthologous variants: 48562744-G-A

182917882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5 prime UTR variant
orthologous variants: 48562744-G-T

http://identifiers.org/hco/4/GRCh38#182917896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48562730-C-A

182917896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2710
most severe consequence: 5 prime UTR variant
orthologous variants: 48562730-C-T