50275667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126468453-A-G

50275894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126468936-G-C

50276012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126469188-G-A

50276201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126469359-G-A

http://identifiers.org/hco/15/GRCh38#50276249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126469398-C-A

50276267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126469416-G-C

50276639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126469741-G-T

50276723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126469821-T-C

50276733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126469829-A-G

http://identifiers.org/hco/15/GRCh38#50276885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126469968-C-A

50276922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126470005-T-C

50277314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126470888-G-T

50277784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126471338-G-A

50277920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126471465-A-G

http://identifiers.org/hco/15/GRCh38#50278447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126471971-C-A

50278447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126471971-C-T

50278511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126472030-A-G

50278511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126472030-A-T

http://identifiers.org/hco/15/GRCh38#50278540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126472059-C-A

50278542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126472061-G-A

50278542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126472061-G-T

50278609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3 prime UTR variant
orthologous variants: 126472128-A-G

50278660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 126472178-C-T

50278721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3_prime_UTR_variant, stop_gained
orthologous variants: 126472239-G-A

50278728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 126472246-A-G

50278850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126472361-T-A

50278850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126472361-T-C

50278850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126472361-T-G

50278921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126472428-T-C

50279047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126472543-T-C

50279274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126472740-T-C

http://identifiers.org/hco/15/GRCh38#50279382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126472834-A-C

50279421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126472873-T-C

http://identifiers.org/hco/15/GRCh38#50279637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126473205-A-C

50279796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126473358-A-G

50279799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126473361-G-C

50279918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126473615-T-C

50279937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126473638-C-T

50280096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126473814-T-G

50280270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126473955-G-C

50280449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126474085-G-A

50280489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126474128-C-T

50281873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126477224-A-G

50282155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126477541-G-A

50282177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126477562-G-A

50282214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126477599-T-A

50282219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126477606-A-G

50282258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126477644-A-G

50282262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126477649-G-A

50282262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126477649-G-T

http://identifiers.org/hco/15/GRCh38#50284140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126478459-C-A

50284140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126478459-C-G

50284858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126479688-T-G

50285241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126480283-G-T

50285297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126480334-G-A

50286002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126481050-A-G

50286003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126481051-G-A

http://identifiers.org/hco/15/GRCh38#50286049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126481130-C-A

50286049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, missense_variant
orthologous variants: 126481130-C-T

50286095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: synonymous variant
orthologous variants: 126481176-T-C

50286204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126481284-T-C

50286275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126481347-A-G

50286305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126481371-A-G

50286409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126481459-T-C

50286848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126481824-C-G

50286872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126481845-A-G

http://identifiers.org/hco/15/GRCh38#50286888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126481849-C-A

50286956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126481928-T-C

50289280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126488365-G-A

50289280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126488365-G-C

50289333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126488419-C-G

50289452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126488453-T-A

50289452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126488453-T-C

50289452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126488453-T-G

50289610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: synonymous variant
orthologous variants: 126488610-T-C

http://identifiers.org/hco/15/GRCh38#50289689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126488697-A-C

50289689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126488697-A-G

50289689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126488697-A-T

http://identifiers.org/hco/15/GRCh38#50289695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126488699-C-A

50289695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126488699-C-G

50289695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126488699-C-T

50289697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126488701-A-G

50289697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126488701-A-T

50290657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126489032-T-C

50291149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126489547-T-G

50293355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126489879-C-T

50294179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126490649-C-T

50300884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: missense variant
orthologous variants: 126492083-G-T

http://identifiers.org/hco/15/GRCh38#50300948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126492145-C-A

50300948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126492145-C-T

50300986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126492180-T-C

50301067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126492261-T-C

http://identifiers.org/hco/15/GRCh38#50301133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126492322-C-A

50301226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126492413-G-A

http://identifiers.org/hco/15/GRCh38#50301475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126492651-C-A

http://identifiers.org/hco/15/GRCh38#50301501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126492674-C-A

50301501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126492674-C-T

50301623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126492792-G-C

50301881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126492895-C-T

50302079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126493063-G-C

50302131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126493081-G-A

http://identifiers.org/hco/15/GRCh38#50302159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126493109-C-A

50302224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126493188-C-T

http://identifiers.org/hco/15/GRCh38#50302805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126494059-C-A

50302805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126494059-C-G

50303005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 126494229-G-A

50303005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 126494229-G-C

50303005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 126494229-G-T

50303073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 126494297-A-G

50303176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126494399-T-A

50303176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126494399-T-C

http://identifiers.org/hco/15/GRCh38#50303819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126495314-C-A

50303819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126495314-C-G

http://identifiers.org/hco/15/GRCh38#50303904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126495404-C-A

50303904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126495404-C-T

50303940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126495449-G-T

50303988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126495497-C-G

50304062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 126495571-A-G

50304066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 126495575-C-G

50304066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 126495575-C-T

http://identifiers.org/hco/15/GRCh38#50304106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126495615-C-A

50304210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126495763-T-C

http://identifiers.org/hco/15/GRCh38#50304229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126495773-C-A

50304229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126495773-C-T

50304302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126495838-A-T

50304358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126495885-T-A

50304358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126495885-T-C

50306963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126497461-T-C

http://identifiers.org/hco/15/GRCh38#50306970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126497468-C-A

50307315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126497757-T-A

50307337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126497783-A-G

50307379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126497818-A-G

50307430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126497860-A-G

50307442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126497873-C-T

50307726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126498124-G-T

50307824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126498213-C-T

50308170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126498479-T-G

50308214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126498522-A-G

50308665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126498878-T-C

50309195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126499644-C-T

http://identifiers.org/hco/15/GRCh38#50309579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126500217-C-A

50309588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126500226-T-C

50309649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126500343-T-A

50309649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126500343-T-C

http://identifiers.org/hco/15/GRCh38#50309651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126500345-A-C

50309655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126500349-G-A

http://identifiers.org/hco/15/GRCh38#50309760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126500459-C-A

50309760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 126500459-C-G

50309760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 126500459-C-T

http://identifiers.org/hco/15/GRCh38#50309802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126500501-A-C

http://identifiers.org/hco/15/GRCh38#50309844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126500539-C-A

50309844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126500539-C-T

50309881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126500565-A-G

50309882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126500566-T-C

50310528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126500850-T-C

50310595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126500911-A-G

50310634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126500951-A-G

http://identifiers.org/hco/15/GRCh38#50310987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126501242-A-C

50311003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126501258-A-G

50312876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126502879-G-T

http://identifiers.org/hco/15/GRCh38#50313498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126503597-C-A

50313866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126504110-G-T

50314015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126504233-A-G

50314209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126504345-A-G

50314216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126504352-C-T

50314221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126504357-T-C

50314385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126504383-G-A

50314385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126504383-G-C

50314385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126504383-G-T

http://identifiers.org/hco/15/GRCh38#50314392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126504390-C-A

50314466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126504456-A-G

http://identifiers.org/hco/15/GRCh38#50314607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126504590-C-A

50315580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126504836-T-A

50315594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126504854-G-A

50342688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126510131-A-G

50342739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126510187-T-A

50346389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126512235-C-T

50346521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126512354-C-T

50346764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126512489-G-A

http://identifiers.org/hco/15/GRCh38#50347223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126512695-C-A

50347639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126513059-G-A

50347639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126513059-G-T

50348094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126513226-C-G

50348094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron variant
orthologous variants: 126513226-C-T

50351772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126514639-T-A

50351801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126514664-T-C

http://identifiers.org/hco/15/GRCh38#50351829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126514692-C-A

50352065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126515030-G-A

50352788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126515346-T-G

http://identifiers.org/hco/15/GRCh38#50352795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126515353-C-A

50352795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126515353-C-T

http://identifiers.org/hco/15/GRCh38#50352908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126515430-C-A

50352929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126515451-A-T

http://identifiers.org/hco/15/GRCh38#50352951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126515476-C-A

50353271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126515755-C-T

50353332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126515801-A-G

50353335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126515804-T-C

50353399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126515854-T-A

50353409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126515864-A-G

50353656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516115-G-A

50353881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516300-A-G

50353881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516300-A-T

50353988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516417-C-T

50354072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516481-T-C

50354266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516664-G-A

50354311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516709-A-G

50354311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516709-A-T

50354393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516735-G-T

50354405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516747-C-G

50354405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516747-C-T

50354434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516775-G-A

50354434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516775-G-C

50354434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516775-G-T

http://identifiers.org/hco/15/GRCh38#50354461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126516807-C-A

50354461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516807-C-T

http://identifiers.org/hco/15/GRCh38#50354468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126516814-C-A

50354468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516814-C-T

50354482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516828-T-C

50354482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516828-T-G

50354488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516829-G-A

50354547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516875-G-A

http://identifiers.org/hco/15/GRCh38#50354577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#126516892-C-A

50354577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126516892-C-T

50354663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126516962-G-A

50354663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126516962-G-C

50354663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126516962-G-T

http://identifiers.org/hco/15/GRCh38#50354695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126516978-A-C

50354695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126516978-A-G

50354793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126517084-G-A

50354793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126517084-G-T

http://identifiers.org/hco/15/GRCh38#50354803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126517094-A-C

50354803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126517094-A-G

50355109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126517398-G-A

50355109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126517398-G-T

http://identifiers.org/hco/15/GRCh38#50355166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#126517455-C-A

50355166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126517455-C-G

50355166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126517455-C-T

50355377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126517644-C-T

http://identifiers.org/hco/15/GRCh38#50355408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#126517674-C-A

50355408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126517674-C-G

50355408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4074
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 126517674-C-T