30080201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4391321-C-T

30080246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4391272-G-T

30080278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4391235-G-C

30080278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4391235-G-T

http://identifiers.org/hco/22/GRCh38#30080461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#4391087-C-A

30080461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4391087-C-T

http://identifiers.org/hco/22/GRCh38#30080518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#4391031-C-A

30080518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 4391031-C-T

30080581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4390982-T-C

http://identifiers.org/hco/22/GRCh38#30081093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4390664-C-A

30081093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4390664-C-T

http://identifiers.org/hco/22/GRCh38#30081136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4390608-C-A

30081136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4390608-C-T

30081138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4390606-G-A

30081138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4390606-G-T

30081141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4390603-C-T

30081144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4390600-T-C

http://identifiers.org/hco/22/GRCh38#30081287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4390452-C-A

30081287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4390452-C-T

30081323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4390418-G-A

30081353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4390387-A-G

30081416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4390323-G-A

http://identifiers.org/hco/22/GRCh38#30081483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4390252-A-C

30081530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4390210-G-A

30081571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4390169-C-G

30081582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4390144-T-C

30081745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4390094-T-G

30081750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4390089-T-A

30081750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4390089-T-C

30081842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4389999-C-T

30085912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4389321-C-T

30086610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4388796-T-C

30087346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4388273-C-T

30088386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4387287-T-G

30088469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4387209-T-C

http://identifiers.org/hco/22/GRCh38#30088883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#4387013-C-A

http://identifiers.org/hco/22/GRCh38#30089192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#4386722-A-C

30089210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 4386704-C-T

30089597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4386516-C-T

http://identifiers.org/hco/22/GRCh38#30089890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4386332-C-A

30089890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4386332-C-T

30090328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4385972-A-G

30090481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4385904-T-C

30090497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4385888-A-G

30093378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4385627-A-G

30093416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4385581-G-A

30093720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4385268-C-T

30093765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4385222-C-T

30093929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 4385074-A-G

30093949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 4385054-T-C

http://identifiers.org/hco/22/GRCh38#30093972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4385031-C-A

30093972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4385031-C-T

30093994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4385009-G-A

30093994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4385009-G-C

30093995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4385008-G-T

30094305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4384740-G-A

30094403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4384658-G-C

30094831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4383626-G-A

http://identifiers.org/hco/22/GRCh38#30098294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4378106-A-C

30098506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4377735-T-C

30098811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4377423-T-C

30098864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4377371-C-T

http://identifiers.org/hco/22/GRCh38#30098870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4377365-C-A

30098884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4377351-G-A

http://identifiers.org/hco/22/GRCh38#30098912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4377323-C-A

30099023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4377212-T-C

http://identifiers.org/hco/22/GRCh38#30099065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4377175-C-A

30099065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4377175-C-T

30099066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4377174-G-A

30099066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4377174-G-T

30102351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4375808-T-C

http://identifiers.org/hco/22/GRCh38#30103475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4374779-C-A

30103475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4374779-C-T

http://identifiers.org/hco/22/GRCh38#30103583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4374708-A-C

http://identifiers.org/hco/22/GRCh38#30103605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4374686-C-A

30103605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4374686-C-T

30104210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4374496-C-T

30104273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4374434-A-G

30104277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4374430-G-T

30104741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4373966-C-G

30104811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4373899-G-A

30104931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4373816-G-C

30104958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4373789-C-T

30104960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4373787-G-T

30105487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4373691-T-A

30105487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4373691-T-C

30105493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4373685-T-C

http://identifiers.org/hco/22/GRCh38#30105501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4373682-A-C

30105501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4373682-A-G

30105501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4373682-A-T

http://identifiers.org/hco/22/GRCh38#30105518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4373669-C-A

30105518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4373669-C-T

30105521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4373666-T-C

30105702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4373483-A-G

30108218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4372676-A-G

30108236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4372658-C-T

30108312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4372582-T-C

30108343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4372551-T-C

30111771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4371628-T-A

30111771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4371628-T-C

30111842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4371565-A-T

http://identifiers.org/hco/22/GRCh38#30111909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4371500-C-A

30111909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4371500-C-T

http://identifiers.org/hco/22/GRCh38#30111910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4371499-C-A

30111910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4371499-C-G

30111910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4371499-C-T

30112371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4370863-G-T

30112379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4370855-T-C

30112387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4370837-T-C

30112527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4370697-G-A

30112527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4370697-G-T

30112577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4370667-A-G

30112577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4370667-A-T

30112646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4370598-G-T

30112971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4370134-G-T

http://identifiers.org/hco/22/GRCh38#30113892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4369536-C-A

30113916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4369513-C-T

30114152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4368852-T-C

30114246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4368762-C-T

30114398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4368263-T-C

30114398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4368263-T-G

30114523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4368132-A-G

30114649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4368011-C-G

30114717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4367943-A-G

30114792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4367879-A-G

30114904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4367802-G-A

30115276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4367335-G-A

30115288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4367324-A-G

http://identifiers.org/hco/22/GRCh38#30115477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4367144-C-A

30116227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4366559-G-A

30116241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4366534-G-A

30116267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4366498-T-C

30116395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4366231-A-G

30117006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4365609-G-A

30117230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4365399-C-T

30117373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4365294-A-G

30117898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4364989-G-A

30119272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4361765-T-G

30119370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4361670-C-T

30119476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4361566-A-G

30119700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4361164-G-A

30119830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4361078-C-G

30120371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4360326-A-T

30120649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4360058-G-A

30120752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4359955-G-A

30120976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4359776-T-C

30121546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4359242-A-T

30121582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4359207-G-T

30121595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4359194-G-A

30121595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4359194-G-T

30121596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4359193-T-C

30121596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4359193-T-G

30121641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 4359153-C-T

http://identifiers.org/hco/22/GRCh38#30121891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4358908-C-A

http://identifiers.org/hco/22/GRCh38#30121949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4358851-C-A

30121949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4358851-C-T

http://identifiers.org/hco/22/GRCh38#30122001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4358804-A-C

30122001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 4358804-A-G

30122021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 4358784-T-G

30122146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: missense variant
orthologous variants: 4358659-G-A

30122176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: missense variant
orthologous variants: 4358629-G-A

30122176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: missense variant
orthologous variants: 4358629-G-C

30122308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4358480-G-A

30122308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4358480-G-T

30122326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4358463-A-T

30122443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4358358-T-C

30122610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4358256-A-T

30123059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4357619-G-C

30123137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4357550-T-C

30123220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4357469-T-C

30149874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4332302-G-T

30150004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4332149-T-A

http://identifiers.org/hco/22/GRCh38#30150182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4331976-C-A

30150232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4331930-A-T

30150706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4331340-C-T

30151340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4331002-A-G

30151426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4330921-G-T

30151483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4330869-A-G

30153553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4329932-G-A

30153579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4329906-C-T

30153590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4329895-T-C

30153598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4329887-G-A

30153958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4329243-A-G

30154065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4328907-G-A

30155925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4327310-T-C

http://identifiers.org/hco/22/GRCh38#30156027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4327185-C-A

30156027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4327185-C-G

30156119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4327106-C-T

30156420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4326826-C-T

30156895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4326392-A-G

30156978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4326313-T-A

http://identifiers.org/hco/22/GRCh38#30157523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4325531-C-A

30157536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4325518-A-G

30157632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4325419-T-C

30157800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4325048-T-G

30159393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4323276-T-C

30159460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4323211-A-T

30159647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4322959-G-C

30160222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4322405-G-A

http://identifiers.org/hco/22/GRCh38#30160775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4321922-C-A

30160776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4321921-T-G

30161436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4320718-G-A

30161493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4320664-T-A

http://identifiers.org/hco/22/GRCh38#30161660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4320352-A-C

30166218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4317063-C-T

30167498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4316610-G-T

30167854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4316305-A-G

30167879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4316288-G-A

30167879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4316288-G-T

30169326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4304445-C-T

30169628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4304198-A-G

30169831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4304081-T-C

30169891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4304060-T-A

30169913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4304038-A-G

30169959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4303993-C-T

http://identifiers.org/hco/22/GRCh38#30170223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4303736-C-A

30170223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4303736-C-T

http://identifiers.org/hco/22/GRCh38#30170276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4303676-C-A

30170448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4303505-A-G

30170858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4303132-A-G

30170971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4303021-T-C

30171250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4302749-C-G

30171362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4302643-C-T

30171377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4302628-G-A

30171465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4302543-C-T

30174123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4299875-G-A

30174208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4298278-G-C

http://identifiers.org/hco/22/GRCh38#30174549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4297960-A-C

30174757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4297741-T-A

http://identifiers.org/hco/22/GRCh38#30174791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4297710-A-C

30175954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4296754-T-A

30175979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4296743-T-G

30175984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4296738-G-A

30175984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4296738-G-T

30176084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, missense_variant
orthologous variants: 4296643-T-C

30176275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4296477-A-G

30176330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4296426-T-G

http://identifiers.org/hco/22/GRCh38#30176335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4296421-C-A

30176335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4296421-C-T

30176383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4296374-G-A

30176383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4296374-G-C

30176584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4296182-A-G

30176687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4296078-T-C

http://identifiers.org/hco/22/GRCh38#30176750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4295992-A-C

30176750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4295992-A-G

30177175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4295496-T-C

30177175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4295496-T-G

30177371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4295291-C-G

30177640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4295053-G-A

30178767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, undefined
orthologous variants: 4294245-A-T

30178768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron variant
orthologous variants: 4294244-T-G

30191987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4271552-C-T

http://identifiers.org/hco/22/GRCh38#30192205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4271381-C-A

30192205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4271381-C-T

30192325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4271294-G-T

30192339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4271285-G-T

30192375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4271254-A-G

30206875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4249662-G-A

30206875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4249662-G-T

http://identifiers.org/hco/22/GRCh38#30206876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4249661-C-A

http://identifiers.org/hco/22/GRCh38#30206886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#4249651-C-A

30206925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4249612-A-G