http://identifiers.org/hco/18/GRCh38#50795256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74015444-C-A

50795256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74015444-C-T

50795298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74015407-G-A

50795400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74015293-T-C

50795488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74015203-G-A

50795488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74015203-G-C

http://identifiers.org/hco/18/GRCh38#50795548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74015138-C-A

http://identifiers.org/hco/18/GRCh38#50795607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74015078-C-A

http://identifiers.org/hco/18/GRCh38#50795609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74015076-C-A

50795609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74015076-C-T

50795610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74015075-T-C

http://identifiers.org/hco/18/GRCh38#50795638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74015050-C-A

http://identifiers.org/hco/18/GRCh38#50795657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74015028-C-A

50795724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014963-G-A

50795724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014963-G-T

50795747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014913-C-G

50795747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014913-C-T

http://identifiers.org/hco/18/GRCh38#50795773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74014887-C-A

50795773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014887-C-G

http://identifiers.org/hco/18/GRCh38#50795812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74014850-C-A

50795812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014850-C-T

50795842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014824-A-G

50795844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014822-A-G

50795844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014822-A-T

http://identifiers.org/hco/18/GRCh38#50795845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74014821-C-A

50795928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014768-A-G

50795943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014750-A-G

50795989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014697-C-T

50796200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014475-A-G

http://identifiers.org/hco/18/GRCh38#50796227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74014449-C-A

50796227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014449-C-T

50797037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014305-T-C

50797081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014261-A-G

50797092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014250-G-T

50797120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014222-C-T

50797178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014164-A-G

50797216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014125-T-C

50797284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74014060-A-G

50797389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74013961-T-C

http://identifiers.org/hco/18/GRCh38#50797394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74013956-C-A

50797606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74013772-G-A

50797606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74013772-G-T

50797607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74013771-T-A

50797607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74013771-T-C

50797649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74013728-A-G

50797650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74013727-G-A

50797650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74013727-G-T

http://identifiers.org/hco/18/GRCh38#50797703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74013677-C-A

50797707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74013673-T-C

50797786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74013603-G-A

50797786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74013603-G-T

50797815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74013579-T-C

50797859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74013541-G-A

http://identifiers.org/hco/18/GRCh38#50797907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74013503-C-A

50798134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: 74013206-A-G

http://identifiers.org/hco/18/GRCh38#50798150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74013136-C-A

50798214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74012874-T-C

50798263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74012826-G-T

50798404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74012632-C-G

http://identifiers.org/hco/18/GRCh38#50798409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74012627-C-A

50798529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74012534-T-C

http://identifiers.org/hco/18/GRCh38#50798690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74011779-C-A

http://identifiers.org/hco/18/GRCh38#50798926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74011600-C-A

50798926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74011600-C-T

http://identifiers.org/hco/18/GRCh38#50798930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74011596-A-C

http://identifiers.org/hco/18/GRCh38#50798938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74011588-A-C

http://identifiers.org/hco/18/GRCh38#50798953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74011564-A-C

50798953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74011564-A-G

50798953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74011564-A-T

50798987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74011530-G-T

50799050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74011483-G-T

50799063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74011469-A-G

50799063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74011469-A-T

http://identifiers.org/hco/18/GRCh38#50799234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74011065-C-A

50799234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74011065-C-T

http://identifiers.org/hco/18/GRCh38#50799294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74011011-C-A

50799294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74011011-C-G

50799294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74011011-C-T

50799304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74011001-C-T

http://identifiers.org/hco/18/GRCh38#50799306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74010999-C-A

50799308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74010997-T-C

50799330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 74010975-T-C

50799414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74010887-G-A

50799414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74010887-G-C

50799485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74010854-G-C

http://identifiers.org/hco/18/GRCh38#50799503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74010836-A-C

50799959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74010685-T-A

50799959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74010685-T-C

50799965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74010679-G-A

50799965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74010679-G-T

50799980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74010664-A-G

http://identifiers.org/hco/18/GRCh38#50799985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74010659-C-A

50799985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74010659-C-T

50799990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74010654-A-G

50799991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74010653-G-A

50799991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 74010653-G-T

50800074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74010568-C-T

http://identifiers.org/hco/18/GRCh38#50800089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74010553-A-C

50800089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74010553-A-G

50800179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74010455-G-C

50800179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74010455-G-T

50800315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74010323-T-A

http://identifiers.org/hco/18/GRCh38#50800356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74010284-C-A

http://identifiers.org/hco/18/GRCh38#50800448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74010215-A-C

50801219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74010034-C-T

50801286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74009969-C-T

50801382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74009874-G-C

50801382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74009874-G-T

50801545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74009714-T-C

http://identifiers.org/hco/18/GRCh38#50801589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74009672-A-C

50801589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74009672-A-G

50802286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74008910-C-T

50802350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74008859-C-T

http://identifiers.org/hco/18/GRCh38#50804653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74007065-A-C

50804654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74007064-G-A

50804654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74007064-G-C

http://identifiers.org/hco/18/GRCh38#50804775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74006937-C-A

50804834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74006876-C-G

50804863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74006807-C-T

50805068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74006568-G-A

50805068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74006568-G-T

50805084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74006552-C-T

50805565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74005866-G-T

50805579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74005852-C-T

50805605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74005828-G-C

50805822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74005597-C-T

50806260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74005415-G-A

50806468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74005233-T-C

50806495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74005208-T-C

http://identifiers.org/hco/18/GRCh38#50806685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74005149-C-A

50806685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74005149-C-T

50806786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 74005051-T-C

http://identifiers.org/hco/18/GRCh38#50806802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74005035-A-C

50806803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74005034-C-G

50806816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74005021-G-T

http://identifiers.org/hco/18/GRCh38#50806844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74004993-A-C

http://identifiers.org/hco/18/GRCh38#50806986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74004762-C-A

http://identifiers.org/hco/18/GRCh38#50807023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74004716-A-C

50807025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74004714-C-G

50807025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74004714-C-T

50807292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74004426-A-G

http://identifiers.org/hco/18/GRCh38#50809174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74003220-C-A

50809174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74003220-C-G

50809174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74003220-C-T

http://identifiers.org/hco/18/GRCh38#50809183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74003211-A-C

50809183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74003211-A-G

50809203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74003191-T-C

50809214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74003180-G-A

50809214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74003180-G-T

http://identifiers.org/hco/18/GRCh38#50809263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74003140-C-A

http://identifiers.org/hco/18/GRCh38#50809357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#74003061-A-C

50809357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74003061-A-G

50809438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74002979-A-G

50809440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74002977-A-G

50809442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74002975-A-G

50809506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74002887-G-A

50809506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74002887-G-T

50812950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74002426-A-G

50813224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74001870-G-A

50813413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74001328-C-G

50814132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74000881-G-A

50816863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74000784-G-A

50816867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74000780-C-G

50816961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74000689-T-C

50817004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74000646-C-G

50817237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73999932-C-T

50817280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73999885-G-A

50818435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73998795-G-T

http://identifiers.org/hco/18/GRCh38#50818562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#73998690-C-A

50818585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73998667-A-G

50819326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73997386-A-G

50819326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73997386-A-T

50819337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73997375-T-C

50819403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73997301-T-C

50819403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 73997301-T-G

50819486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73997211-G-A

50819486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73997211-G-T

50819625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 73997083-T-C

50819633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 73997071-T-A

50819658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 73997043-T-C

50819745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 73996950-T-G

50819830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73996871-G-C

50819830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73996871-G-T

50820051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73996664-T-A

50820051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73996664-T-G

http://identifiers.org/hco/18/GRCh38#50820053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#73996662-C-A

50820053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 73996662-C-T

50820087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, undefined
orthologous variants: 73996627-G-A

50820087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, undefined
orthologous variants: 73996627-G-T

50820150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, undefined
orthologous variants: 73996586-T-A

50820150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, undefined
orthologous variants: 73996586-T-C

50820150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, undefined
orthologous variants: 73996586-T-G

50820540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: 73996170-A-T

http://identifiers.org/hco/18/GRCh38#50821661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#73994851-C-A

50821845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: 73994672-T-C

50821854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: 73994668-T-C

50822865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: 73993946-G-A

50822869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: 73993942-G-C

http://identifiers.org/hco/18/GRCh38#50822877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#73993934-C-A

50823224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: 73993682-C-T

50823297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: 73993614-G-A

http://identifiers.org/hco/18/GRCh38#50823375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#73993541-C-A

50823376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: 73993540-G-A

50823376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: 73993540-G-T

50823484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: 73993440-T-A

50823582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993393-T-G

50823701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993292-A-G

50823724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993269-A-T

http://identifiers.org/hco/18/GRCh38#50823789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#73993217-C-A

50823789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993217-C-T

50823790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993216-A-G

50823832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993166-A-G

50823832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993166-A-T

50823833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993165-T-C

50823877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993144-T-C

http://identifiers.org/hco/18/GRCh38#50823879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#73993142-C-A

50823879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993142-C-T

http://identifiers.org/hco/18/GRCh38#50823887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#73993134-C-A

50823887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993134-C-G

50823887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993134-C-T

50823898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993123-G-A

50823898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993123-G-T

50823909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993090-G-A

50823909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993090-G-T

50823911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993088-A-G

50823936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73993063-A-G

50824058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73992961-T-C

http://identifiers.org/hco/18/GRCh38#50824068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#73992937-C-A

50824071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73992934-G-C

50824071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73992934-G-T

50824077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73992928-G-A

http://identifiers.org/hco/18/GRCh38#50824110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#73992905-C-A

50824110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73992905-C-T

50824128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: 73992887-A-G

50825271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: 73992563-A-T

http://identifiers.org/hco/18/GRCh38#50825300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#73992534-C-A

50825300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: intron variant
orthologous variants: 73992534-C-T

50825348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5 prime UTR variant
orthologous variants: 73992486-T-A

50825348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5 prime UTR variant
orthologous variants: 73992486-T-C

50825348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5 prime UTR variant
orthologous variants: 73992486-T-G

50825397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24121
most severe consequence: 5 prime UTR variant
orthologous variants: 73992439-A-G