43353700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 5 prime UTR variant
orthologous variants: 24459726-A-G

43353719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24459705-G-C

43353752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24459672-T-A

43353800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24459623-T-C

43353883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24459535-C-G

43353883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24459535-C-T

43353884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 24459534-A-G

43353884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 24459534-A-T

43353952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24459463-G-A

43353954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24459461-G-A

http://identifiers.org/hco/19/GRCh38#43354021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24459395-C-A

43354021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24459395-C-T

43354051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24459365-G-C

http://identifiers.org/hco/19/GRCh38#43354073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24459330-C-A

43354073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24459330-C-T

http://identifiers.org/hco/19/GRCh38#43354098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24459322-C-A

43354098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24459322-C-G

43354098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24459322-C-T

http://identifiers.org/hco/19/GRCh38#43354173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24459247-C-A

http://identifiers.org/hco/19/GRCh38#43354175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24459245-C-A

43354175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24459245-C-G

http://identifiers.org/hco/19/GRCh38#43354243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24459173-C-A

43354243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24459173-C-G

43354243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24459173-C-T

43354264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24459152-C-G

43354344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24459072-A-G

43354374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24459042-G-A

43354382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 24459034-G-A

43354398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 24459003-T-G

43354401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 24459000-G-A

43354401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 24459000-G-C

43354401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 24459000-G-T

43354404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 24458997-A-G

http://identifiers.org/hco/19/GRCh38#43354481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24458914-C-A

http://identifiers.org/hco/19/GRCh38#43354495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24458900-C-A

43354495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 24458900-C-G

43354495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 24458900-C-T

http://identifiers.org/hco/19/GRCh38#43354496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24458899-C-A

43354496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 24458899-C-G

43354496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 24458899-C-T

http://identifiers.org/hco/19/GRCh38#43354526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24458869-C-A

43354526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24458869-C-G

43354526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24458869-C-T

http://identifiers.org/hco/19/GRCh38#43354562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24458851-C-A

43354562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24458851-C-T

43354762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24458599-G-A

43354762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24458599-G-C

43355241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24458209-G-A

43355241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24458209-G-T

http://identifiers.org/hco/19/GRCh38#43355253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24458197-A-C

43355342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24458117-G-C

http://identifiers.org/hco/19/GRCh38#43355408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24458066-A-C

43355408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24458066-A-G

43355408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24458066-A-T

43355426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24458047-T-C

43355452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24458030-G-T

43355465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24458013-T-C

43355465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24458013-T-G

http://identifiers.org/hco/19/GRCh38#43355504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24457980-C-A

43355504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24457980-C-T

http://identifiers.org/hco/19/GRCh38#43355519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24457960-C-A

43355519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 24457960-C-T

http://identifiers.org/hco/19/GRCh38#43355540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24457939-C-A

43355540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 24457939-C-T

43355545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 24457934-T-A

43355545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 24457934-T-C

43355545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 24457934-T-G

43355551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 24457928-A-G

http://identifiers.org/hco/19/GRCh38#43355554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24457925-C-A

43355554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 24457925-C-T

43355640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 24457891-C-T

43355648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 24457883-G-A

43355660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_acceptor_variant
orthologous variants: 24457873-G-C

43355720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 24457816-A-G

43355757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 24457779-A-G

43355758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 24457778-T-C

43355798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24457740-T-C

43355798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24457740-T-G

43355820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24457719-A-G

43355868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24457680-G-A

43355868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24457680-G-C

43355868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24457680-G-T

http://identifiers.org/hco/19/GRCh38#43355869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24457679-C-A

43355869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24457679-C-T

43355958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24457593-A-G

43355963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24457588-T-A

http://identifiers.org/hco/19/GRCh38#43355980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24457571-C-A

43355980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24457571-C-G

43355980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24457571-C-T

http://identifiers.org/hco/19/GRCh38#43355981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24457570-C-A

43355981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24457570-C-G

http://identifiers.org/hco/19/GRCh38#43356048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24453759-C-A

http://identifiers.org/hco/19/GRCh38#43356069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24453738-A-C

43356069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 24453738-A-G

43356069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 24453738-A-T

http://identifiers.org/hco/19/GRCh38#43356075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24453732-C-A

43356075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 24453732-C-T

43356128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24453669-T-G

43356151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24453646-G-A

43356177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24453624-A-G

43356514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24452216-G-C

43356855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24451911-T-A

43359936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24445992-T-C

43359947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24445981-A-G

43359994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24445934-G-C

http://identifiers.org/hco/19/GRCh38#43360059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24445898-C-A

43360076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24445881-C-G

43360076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24445881-C-T

http://identifiers.org/hco/19/GRCh38#43360143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24445808-A-C

43360143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24445808-A-T

43360166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24445785-T-C

43360176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24445775-G-C

43360176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24445775-G-T

43360195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24445758-A-G

43360264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, splice_acceptor_variant
orthologous variants: 24445687-G-T

43360314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 24445631-G-T

http://identifiers.org/hco/19/GRCh38#43360319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24445626-A-C

43360407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: 24445538-T-C

43360417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24445528-G-C

43360417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24445528-G-T

43360438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24445507-T-C

http://identifiers.org/hco/19/GRCh38#43360491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24445478-C-A

http://identifiers.org/hco/19/GRCh38#43360507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24445463-C-A

43360533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24445438-T-C

43360815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24445076-G-A

43360815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24445076-G-T

43360876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444964-G-A

43360876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444964-G-C

43360876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444964-G-T

43360884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444956-G-A

43360884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444956-G-T

http://identifiers.org/hco/19/GRCh38#43360902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24444921-C-A

43360902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444921-C-G

43360902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444921-C-T

43360914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444904-T-C

43360914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444904-T-G

http://identifiers.org/hco/19/GRCh38#43360915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24444903-C-A

43360915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444903-C-G

43360915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444903-C-T

43360919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444899-G-A

43360919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444899-G-C

43360919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444899-G-T

http://identifiers.org/hco/19/GRCh38#43360943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24444865-C-A

43360943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444865-C-G

43360943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444865-C-T

http://identifiers.org/hco/19/GRCh38#43360955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24444848-A-C

43360955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444848-A-T

43360956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444847-G-A

43360956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444847-G-C

43360956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444847-G-T

http://identifiers.org/hco/19/GRCh38#43360980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24444827-C-A

43360980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444827-C-G

43360980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444827-C-T

43361003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444806-T-A

43361005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444804-A-G

43361017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444791-C-G

43361054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444750-T-G

43361062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444744-A-G

http://identifiers.org/hco/19/GRCh38#43361124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24444699-C-A

43361124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444699-C-G

43361124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444699-C-T

43361166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 24444654-A-T

43361186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 24444634-T-G

43361190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 24444630-G-A

43361190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 24444630-G-T

43361192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 24444628-T-G

43361296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 24444524-G-A

43361307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 24444513-C-T

43361358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444467-G-A

43361508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 24444322-G-A

43361508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 24444322-G-C

43361606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444230-G-T

http://identifiers.org/hco/19/GRCh38#43361668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24444178-C-A

43361668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444178-C-T

http://identifiers.org/hco/19/GRCh38#43361782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24444077-C-A

43361782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444077-C-G

43361790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444069-G-A

43361808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444052-G-A

http://identifiers.org/hco/19/GRCh38#43361809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24444051-A-C

43361809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444051-A-G

43361919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24444010-G-A

43361980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24443961-T-C

43361980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24443961-T-G

43361982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24443959-T-A

43361982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24443959-T-C

43361985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24443956-G-A

43361985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24443956-G-C

43361985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24443956-G-T

43362027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24443935-G-A

43362027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24443935-G-C

43362043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24443921-T-A

43362043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24443921-T-C

43362058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24443905-G-A

43362080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 24443884-C-T

43362097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 24443867-C-T

43362208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 24443771-C-G

43362273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 24443688-G-A

http://identifiers.org/hco/19/GRCh38#43362332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24443630-C-A

43362332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24443630-C-T

http://identifiers.org/hco/19/GRCh38#43362389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24443573-C-A

43362389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24443573-C-T

43362400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24443564-G-C

http://identifiers.org/hco/19/GRCh38#43362402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24443562-A-C

43362402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24443562-A-G

43362411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24443557-T-C

http://identifiers.org/hco/19/GRCh38#43362418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24443550-C-A

43362418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24443550-C-T

http://identifiers.org/hco/19/GRCh38#43362419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24443549-A-C

43362419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24443549-A-G

43362424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24443544-G-A

http://identifiers.org/hco/19/GRCh38#43362443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24443525-C-A

43362443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24443525-C-T

43362456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24443518-T-A

43362456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24443518-T-C

43362546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30072
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 24443441-A-G