58237634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5 prime UTR variant
orthologous variants: 14467040-G-A

58237634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5 prime UTR variant
orthologous variants: 14467040-G-T

58237681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5 prime UTR variant
orthologous variants: 14466997-C-G

58237681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5 prime UTR variant
orthologous variants: 14466997-C-T

58237692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5 prime UTR variant
orthologous variants: 14466986-C-T

58237693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5 prime UTR variant
orthologous variants: 14466985-G-A

58237693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5 prime UTR variant
orthologous variants: 14466985-G-T

58237696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 14466982-G-A

58237696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 14466982-G-T

58237716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5 prime UTR variant
orthologous variants: 14466971-G-T

58237762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5 prime UTR variant
orthologous variants: 14466924-C-T

58237827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5 prime UTR variant
orthologous variants: 14466860-G-A

http://identifiers.org/hco/3/GRCh38#58237896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14466819-C-A

58237929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14466787-G-A

58237929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14466787-G-C

58237929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14466787-G-T

http://identifiers.org/hco/3/GRCh38#58238011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14466676-C-A

58238011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14466676-C-T

58238038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 14466645-A-T

58238152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 14466529-C-T

http://identifiers.org/hco/3/GRCh38#58238280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14466407-C-A

58238280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14466407-C-G

58238280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14466407-C-T

58238565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 14465354-T-C

58238595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 14465324-A-G

http://identifiers.org/hco/3/GRCh38#58238708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14465239-C-A

58238708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14465239-C-T

58238959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14465029-G-C

58239178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14464591-A-T

58241139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14461301-G-C

58241467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14461075-G-A

58241606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14460948-A-G

58241853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14460716-T-C

58241974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14460646-G-A

58241998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14460623-C-G

58242084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14460539-G-A

58242124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14460524-T-A

58242125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14460523-G-C

58242156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14460498-G-A

58242286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14460382-G-A

58242591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14460122-G-T

58244945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14457611-G-A

58244945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14457611-G-T

58245018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14457537-A-G

58246120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14457214-C-T

58246166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14457171-G-A

58246166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14457171-G-C

58246166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14457171-G-T

58246280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14457059-T-C

http://identifiers.org/hco/3/GRCh38#58246301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14457038-C-A

58246596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14456764-G-A

58246691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14456690-C-T

58246886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14456518-T-C

58246912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14456488-G-A

58248719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14454308-A-G

58248722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14454305-A-G

58249194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14453829-T-C

58249585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14453428-C-G

58249661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 14453319-C-G

58249997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14452987-A-G

58250311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14452729-C-T

58250971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14450590-A-G

58251384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14445882-T-G

58251476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14445792-C-T

58251658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14445610-G-A

58252103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14445137-C-T

58252144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14445109-G-A

58252190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14445042-G-A

58252225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14444918-G-C

58252225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14444918-G-T

58252259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14444883-G-A

58252259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14444883-G-T

58252600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14444167-A-G

58252600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14444167-A-T

http://identifiers.org/hco/3/GRCh38#58252694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14444094-A-C

58252694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14444094-A-G

58252912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14443899-A-G

58253007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14443067-A-G

58253153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14442950-C-G

58253165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14442942-G-T

58253495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14442642-C-T

58253525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14442612-T-C

http://identifiers.org/hco/3/GRCh38#58256111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14441933-A-C

58256300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14441739-C-T

58256333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14441707-G-A

58256460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14441621-A-T

58256470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14441611-T-C

http://identifiers.org/hco/3/GRCh38#58256499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14441586-C-A

58256499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14441586-C-T

58256802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14441291-G-A

58257753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14440979-C-T

58258432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 14439335-T-C

58258464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 14439306-A-G

58258464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 14439306-A-T

http://identifiers.org/hco/3/GRCh38#58258531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14439249-A-C

58258612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 14439183-C-T

58258622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 14439173-T-C

http://identifiers.org/hco/3/GRCh38#58258715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14439089-C-A

58258715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14439089-C-G

58258769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14439035-G-A

58258769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14439035-G-T

58259076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14438758-C-T

58260142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14437786-G-C

58260194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14437737-C-G

58260228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14437703-G-A

58260341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14437593-C-G

58260656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14437281-A-T

58260748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14437191-G-T

58260776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14437166-G-T

58261038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14436933-T-C

58261074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14436893-T-C

58261135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14436832-A-G

58261288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14436697-G-A

http://identifiers.org/hco/3/GRCh38#58261307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14436679-A-C

58265293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14431831-T-C

58265359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14431765-G-T

http://identifiers.org/hco/3/GRCh38#58265377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14431752-A-C

58265976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14431189-G-C

58266146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14431031-T-C

58266507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14430919-G-A

58266530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14430889-T-C

58266530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14430889-T-G

58266550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14430870-A-G

58266679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14430665-A-G

58266679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14430665-A-T

http://identifiers.org/hco/3/GRCh38#58267070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14430135-C-A

58267075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14430129-G-A

58267075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14430129-G-T

58267124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14430080-C-T

58267167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14430038-C-G

58267167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 14430038-C-T

58267357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429856-G-A

58267357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429856-G-C

58267360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429853-T-C

58267360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429853-T-G

58267376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429843-A-G

58267376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429843-A-T

58268131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429757-T-A

58268158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429730-C-T

58268184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429704-C-T

58268216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429659-A-G

58268248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429623-T-C

58268541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429345-G-C

58268689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429215-G-A

58268747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429182-T-C

58268763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429166-G-A

http://identifiers.org/hco/3/GRCh38#58268814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14429120-A-C

58268814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429120-A-G

58268971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429014-T-C

58268972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14429013-G-C

58269095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428891-C-T

http://identifiers.org/hco/3/GRCh38#58269190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14428794-C-A

58269190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428794-C-T

58269232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428759-G-A

58269232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428759-G-T

58269241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428748-A-T

58269244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428745-T-C

58269246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428742-G-A

58269246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428742-G-T

58269266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428717-G-T

58269270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428713-A-G

58269284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428687-C-T

http://identifiers.org/hco/3/GRCh38#58269293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14428678-C-A

58269312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428659-T-C

58269312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428659-T-G

http://identifiers.org/hco/3/GRCh38#58269377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14428596-C-A

58269413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: synonymous variant
orthologous variants: 14428560-G-T

58269445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428528-G-A

http://identifiers.org/hco/3/GRCh38#58269453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14428520-C-A

58269453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428520-C-G

58269453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428520-C-T

58269474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428499-C-T

58269550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428442-T-G

http://identifiers.org/hco/3/GRCh38#58269573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14428419-C-A

58269573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428419-C-T

58269587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14428405-G-T

58269984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427849-C-T

58270011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427679-C-T

58270076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427597-C-G

58270076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427597-C-T

58270317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427456-T-G

58270341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427432-C-T

58270344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427429-A-G

http://identifiers.org/hco/3/GRCh38#58270480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14427297-A-C

http://identifiers.org/hco/3/GRCh38#58270783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14427201-C-A

58270820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427161-C-G

58270837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427152-T-A

58270838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427151-G-A

58270838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427151-G-C

58270850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427139-T-G

58270854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427137-G-T

58270870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427121-T-C

http://identifiers.org/hco/3/GRCh38#58270889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14427115-C-A

58270889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427115-C-T

58270899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427110-A-G

http://identifiers.org/hco/3/GRCh38#58270904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14427105-C-A

58270904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14427105-C-G

58270957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: missense variant
orthologous variants: 14427052-A-G

http://identifiers.org/hco/3/GRCh38#58271051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14426958-C-A

58271051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: synonymous variant
orthologous variants: 14426958-C-T

http://identifiers.org/hco/3/GRCh38#58271207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14426801-C-A

58271228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14426780-T-A

58271272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14426738-T-A

58271283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14426727-T-C

58271686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14425643-T-A

58271686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14425643-T-C

58272401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron_variant, undefined
orthologous variants: 14425421-T-C

http://identifiers.org/hco/3/GRCh38#58272412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14425411-C-A

58272412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron_variant, undefined
orthologous variants: 14425411-C-G

http://identifiers.org/hco/3/GRCh38#58272611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14424842-A-C

58272611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14424842-A-G

http://identifiers.org/hco/3/GRCh38#58274553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14424401-C-A

58274594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14424365-A-G

58274604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14424355-G-T

58274623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14424336-T-C

58274623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14424336-T-G

58274647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14424312-G-T

58274695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: synonymous variant
orthologous variants: 14424266-G-A

58274695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: synonymous variant
orthologous variants: 14424266-G-T

http://identifiers.org/hco/3/GRCh38#58274743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14424218-C-A

http://identifiers.org/hco/3/GRCh38#58274839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14424126-C-A

58274839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14424126-C-T

58274856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14424106-G-A

58274856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14424106-G-T

http://identifiers.org/hco/3/GRCh38#58274888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14424089-A-C

58274888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14424089-A-G

58274918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14424058-T-C

58275026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14423967-C-T

58282791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14423076-G-C

58283001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14422860-T-C

58283143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14422727-G-A

58283977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14421658-A-G

58283977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14421658-A-T

58284248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14421420-G-C

58284449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14421323-A-T

58284625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14421162-C-T

58284635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14421155-G-T

58284819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14420999-T-A

http://identifiers.org/hco/3/GRCh38#58284933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14420339-C-A

58284933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14420339-C-G

58284944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14420328-G-T

58284953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14420319-G-A

58284953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14420319-G-C

58285006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron variant
orthologous variants: 14420276-A-G

58285102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: synonymous variant
orthologous variants: 14420180-C-T

http://identifiers.org/hco/3/GRCh38#58285126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14420156-C-A

58285126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: synonymous variant
orthologous variants: 14420156-C-T

58285201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14420099-T-C

58285372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 14419944-T-G

http://identifiers.org/hco/3/GRCh38#58285432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14419884-C-A

58285432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 14419884-C-G

58285502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14419845-G-T

58293600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 14414289-G-A

58293760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: missense variant
orthologous variants: 14414132-G-A

58293778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: 14414114-A-G

58293781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: 14414111-C-G

http://identifiers.org/hco/3/GRCh38#58293895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14413997-C-A

58293895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: 14413997-C-T

http://identifiers.org/hco/3/GRCh38#58293949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14413944-C-A

58293949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: 14413944-C-G

http://identifiers.org/hco/3/GRCh38#58294038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14413837-C-A

58294038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: 14413837-C-T

http://identifiers.org/hco/3/GRCh38#58294040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14413835-C-A

58294040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: 14413835-C-T

http://identifiers.org/hco/3/GRCh38#58294057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14413818-A-C

58294057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: 14413818-A-G

http://identifiers.org/hco/3/GRCh38#58294062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14413813-C-A

58294062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: 14413813-C-T

http://identifiers.org/hco/3/GRCh38#58294108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14413769-C-A

58294108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: 14413769-C-T

58294124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: 14413753-T-A

58294127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: 14413742-A-T

58294247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: 14413624-T-C

http://identifiers.org/hco/3/GRCh38#58294292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14413578-C-A

58294292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: 14413578-C-T

http://identifiers.org/hco/3/GRCh38#58294316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14413539-C-A

http://identifiers.org/hco/3/GRCh38#58294317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14413538-A-C

58294317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21398
most severe consequence: 3 prime UTR variant
orthologous variants: 14413538-A-G