84999299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5 prime UTR variant
orthologous variants: 145853046-A-G

84999300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5 prime UTR variant
orthologous variants: 145853045-A-G

http://identifiers.org/hco/1/GRCh38#84999305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145853040-C-A

84999305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5 prime UTR variant
orthologous variants: 145853040-C-T

84999318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5 prime UTR variant
orthologous variants: 145853027-T-C

84999345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 145853003-A-G

84999345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 145853003-A-T

84999355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852993-T-C

84999382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852968-G-A

84999382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852968-G-T

84999385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852965-A-G

84999385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852965-A-T

84999401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852949-G-T

84999429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852909-G-A

84999466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852863-A-G

84999506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852831-A-T

http://identifiers.org/hco/1/GRCh38#84999601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145852762-C-A

84999601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852762-C-T

84999739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852641-T-C

84999747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852632-A-G

84999804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852576-T-C

84999806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852574-T-G

84999863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852510-G-A

85000273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852426-G-A

85000273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852426-G-C

85000423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852272-C-T

85000424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145852271-T-C

85000734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145851995-G-A

85000942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145851774-C-G

85000944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145851772-A-G

http://identifiers.org/hco/1/GRCh38#85000949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145851765-C-A

85000951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145851763-T-C

85017070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145847436-G-A

85017101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145847402-C-T

85017119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145847382-C-G

85017119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145847382-C-T

85017986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145847001-G-A

http://identifiers.org/hco/1/GRCh38#85017987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145847000-C-A

85017987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145847000-C-T

85018108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 145846880-T-G

http://identifiers.org/hco/1/GRCh38#85018145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145846844-C-A

http://identifiers.org/hco/1/GRCh38#85018897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145846569-C-A

85018897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 145846569-C-G

85018934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 145846532-T-A

85018954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 145846513-G-T

85019112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 145846362-A-G

85019156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 145846318-A-T

85019537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145845954-G-A

85019684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145845808-G-T

85021125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 145845275-T-C

85021138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 145845262-T-C

85021302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145845099-A-T

85021306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145845095-T-G

85021371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145845041-A-G

85021380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145845032-G-T

85021382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145845030-T-C

85021407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145845005-G-A

85021433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145844981-T-C

85021433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145844981-T-G

85021612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145844587-A-G

85021852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145844397-G-A

85021932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145844292-A-T

85021990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145844234-G-A

85021990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145844234-G-T

85022093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 145843299-C-T

85022110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 145843282-C-G

85022134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 145843258-G-A

85022194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, splice_acceptor_variant, undefined
orthologous variants: 145843198-T-G

85022351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 145843060-A-G

85022354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 145843057-G-A

85022559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842823-G-A

85022559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842823-G-T

http://identifiers.org/hco/1/GRCh38#85022628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145842753-A-C

85022644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842730-G-A

http://identifiers.org/hco/1/GRCh38#85022695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145842661-C-A

85022702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842654-G-A

http://identifiers.org/hco/1/GRCh38#85022743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145842621-C-A

85022744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842620-T-C

85022747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842617-G-A

85022921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842431-A-G

85022948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842406-A-G

85022959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842395-G-T

85022968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842390-G-T

85022969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842389-A-G

85023064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842344-G-T

http://identifiers.org/hco/1/GRCh38#85023289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145842316-C-A

85023289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842316-C-T

http://identifiers.org/hco/1/GRCh38#85023332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145842304-C-A

85023424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842259-G-T

http://identifiers.org/hco/1/GRCh38#85023446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145842237-A-C

85023477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842214-A-G

85023478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842213-G-A

85023501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145842186-A-G

http://identifiers.org/hco/1/GRCh38#85023506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145842181-A-C

http://identifiers.org/hco/1/GRCh38#85023517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145842170-C-A

http://identifiers.org/hco/1/GRCh38#85023529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145842159-C-A

85023529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145842159-C-T

85023532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145842156-G-A

85023532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145842156-G-T

85023537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145842151-G-A

85023537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145842151-G-T

85023610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145842082-T-A

85023662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145842040-T-C

85023665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145842037-A-G

http://identifiers.org/hco/1/GRCh38#85023817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145841888-C-A

85023964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145841785-T-C

http://identifiers.org/hco/1/GRCh38#85023965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145841784-C-A

http://identifiers.org/hco/1/GRCh38#85024204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145841661-C-A

85024204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145841661-C-G

85024204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145841661-C-T

85024319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145841546-G-A

85024346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145841524-T-C

85024526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145841399-T-G

85024696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 145841222-G-T

85024702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 145841216-A-G

http://identifiers.org/hco/1/GRCh38#85024805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145841058-C-A

85024805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 145841058-C-T

http://identifiers.org/hco/1/GRCh38#85024875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145840997-C-A

85024880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145840995-A-G

http://identifiers.org/hco/1/GRCh38#85024882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145840993-C-A

http://identifiers.org/hco/1/GRCh38#85024892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145840979-C-A

85024892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145840979-C-T

85024912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145840962-G-A

http://identifiers.org/hco/1/GRCh38#85024920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145840954-C-A

85024920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145840954-C-T

http://identifiers.org/hco/1/GRCh38#85024929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145840945-C-A

85025008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145840867-T-C

http://identifiers.org/hco/1/GRCh38#85025179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145840706-C-A

85025381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145840546-T-C

85025395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145840530-G-T

85025509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145840426-C-T

http://identifiers.org/hco/1/GRCh38#85025546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145840330-C-A

85025546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145840330-C-T

85025642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 145840232-G-A

85025642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 145840232-G-T

http://identifiers.org/hco/1/GRCh38#85025669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145840220-C-A

85025669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 145840220-C-T

85025687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 145840202-T-C

85025724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 145840185-A-T

85025735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 145840172-A-G

http://identifiers.org/hco/1/GRCh38#85025809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145839844-C-A

85025809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839844-C-G

85025840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839813-A-G

http://identifiers.org/hco/1/GRCh38#85025889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145839777-C-A

85025955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 145839726-A-G

85026072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 145839609-A-T

85026120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839563-G-A

85026128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839555-C-T

85026346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839355-T-A

85026346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839355-T-C

85026433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839271-A-G

85026434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839270-G-C

85026614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839177-G-A

85026614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839177-G-T

85026648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839146-T-A

85026648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839146-T-C

85026649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839145-T-C

85026742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839060-G-A

85026755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839047-T-A

85026755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839047-T-C

85026787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839026-T-A

85026787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145839026-T-C

85027108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145838953-T-G

85027177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145838885-C-T

85027242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145838811-G-C

85027305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145838755-T-C

85027452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145838618-T-A

85027625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145838459-A-G

85028049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145837897-A-G

85028501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145837538-G-A

85028679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145837370-T-G

85028689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145837363-C-T

85028768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145837270-T-C

85028878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145837214-T-C

85029014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145837085-T-C

85029014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145837085-T-G

85029150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 145836955-T-A

85029150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 145836955-T-C

85029173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 145836932-T-A

http://identifiers.org/hco/1/GRCh38#85029308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145836795-C-A

http://identifiers.org/hco/1/GRCh38#85029346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145836753-C-A

85029454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145836647-T-C

http://identifiers.org/hco/1/GRCh38#85029611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145836514-C-A

85029745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145836361-A-T

http://identifiers.org/hco/1/GRCh38#85029797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145836315-C-A

85029797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145836315-C-T

85029836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145836263-T-C

85029864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145836230-A-T

85029870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145836224-G-T

85029896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145836199-C-G

85029930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145835699-A-G

http://identifiers.org/hco/1/GRCh38#85029981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145835653-C-A

85029981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145835653-C-T

85030047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145835586-T-C

http://identifiers.org/hco/1/GRCh38#85030073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145835560-C-A

85030073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145835560-C-T

85030352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145835311-A-T

85030404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145835259-A-G

85032447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145835181-G-A

85032499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145835132-G-C

85032552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145835085-G-A

http://identifiers.org/hco/1/GRCh38#85032553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145835084-A-C

85032553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145835084-A-T

85032588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145835053-A-G

85032733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 145834908-T-A

85032821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145834794-T-C

85032821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145834794-T-G

85032852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145834740-C-T

http://identifiers.org/hco/1/GRCh38#85032859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145834733-C-A

85032912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 145834680-G-A

85032912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 145834680-G-C

85032998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145834606-A-G

85033106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145834523-T-C

85033108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145834521-G-T

85033946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145834162-A-T

85033961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145834147-A-T

http://identifiers.org/hco/1/GRCh38#85034008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145834100-C-A

85034008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145834100-C-G

85034057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145834050-G-A

85034057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145834050-G-T

85034075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145834032-T-G

85034348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145833753-C-G

85037993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145833442-G-A

85039507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145833198-T-G

85040199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145831810-C-G

85040220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145831789-T-A

85040244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145831766-T-A

85040250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145831760-C-T

85040306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145831681-A-G

85040307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145831680-C-T

85040394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145831596-G-A

85040394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145831596-G-T

85040540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145831460-A-G

85040558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145831442-T-C

85040787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145831228-G-A

85040787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145831228-G-T

85040856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145831143-A-T

85040999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145830781-A-G

85041016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 145830659-T-C

85041078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 145830597-T-C

85041078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 145830597-T-G

85041216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145830461-T-C

85041221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145830456-G-A

85041221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145830456-G-T

85042985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145829608-C-T

85043017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145829586-T-A

85043017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145829586-T-C

85043050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145829552-G-C

85043112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145829490-G-T

85043678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145829249-C-G

85044029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145829112-C-T

85044174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145828987-G-A

85044266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145828918-A-G

85044424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145828794-A-G

http://identifiers.org/hco/1/GRCh38#85044646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145828408-C-A

85044665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145828390-C-T

85044681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145828374-A-G

85044822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145828222-T-C

85044999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145827893-T-A

85044999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145827893-T-C

85045056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145827841-A-T

85045106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145827800-A-G

85045121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145827785-T-G

85045305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 145827601-C-T

85045323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 145827583-G-A

85045323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 145827583-G-C

85045461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145827457-A-G

85045461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145827457-A-T

85045535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145826601-G-A

85045615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145826515-A-G

85045655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145826442-T-A

85045792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145826293-A-G

85046042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145826121-A-G

85046161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145826012-G-A

85046277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145825906-G-C

85046552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145825647-G-C

http://identifiers.org/hco/1/GRCh38#85046572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145825627-A-C

85046625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145825584-T-A

85046625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145825584-T-C

85046645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145825564-A-G

85046694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145825515-C-T

85046719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145825490-A-G

85046760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145825448-A-G

85047034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145825180-T-C

85048100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145823672-G-C

http://identifiers.org/hco/1/GRCh38#85048168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145823613-A-C

85048193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 145823593-G-T

85048195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 145823591-C-T

85048258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145823522-G-A

85048258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145823522-G-T

85048278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145823500-G-A

85048278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145823500-G-T

85048282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145823496-T-C

http://identifiers.org/hco/1/GRCh38#85048328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145823456-C-A

85048328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145823456-C-T

http://identifiers.org/hco/1/GRCh38#85048331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145823453-C-A

85048331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145823453-C-G

85048412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 145823360-A-G

http://identifiers.org/hco/1/GRCh38#85048414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145823358-C-A

85048414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 145823358-C-T

85048428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 145823344-G-C

85048430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 145823342-G-A

http://identifiers.org/hco/1/GRCh38#85048500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145823259-C-A

85048500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 145823259-C-T

85048605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145823171-G-T

85048611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145823165-C-G

85048611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145823165-C-T

85048670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145823103-G-A

85048670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145823103-G-C

http://identifiers.org/hco/1/GRCh38#85048950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145822865-C-A

85049270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145821819-A-T

85049735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145821278-C-T

85056651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145818856-C-T

85056720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145818792-C-T

85057430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145818058-T-A

85057951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145817593-T-C

85057966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145817574-T-C

85057992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145817543-C-T

http://identifiers.org/hco/1/GRCh38#85057999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145817536-A-C

85058020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145817515-A-G

85058023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145817512-A-G

http://identifiers.org/hco/1/GRCh38#85058070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145817494-C-A

85058085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145817479-A-G

85058110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145817454-T-G

85058239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145817363-A-G

85058588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145816716-A-G

85058629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145816668-C-T

85058849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145816464-C-G

85058881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145816434-T-C

85059053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145816273-C-G

85059202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145816136-C-T

85059572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145815829-T-C

85059597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145815804-T-A

http://identifiers.org/hco/1/GRCh38#85059644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145815760-A-C

http://identifiers.org/hco/1/GRCh38#85059725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145815676-C-A

85060075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145815429-C-T

85060113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145815402-G-C

85060200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145815324-T-A

85060453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145815094-A-G

85061724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145814420-G-A

http://identifiers.org/hco/1/GRCh38#85061979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145814134-C-A

85061979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145814134-C-T

85062044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145814110-A-T

http://identifiers.org/hco/1/GRCh38#85062053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145814101-C-A

http://identifiers.org/hco/1/GRCh38#85062194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145813962-C-A

85062194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145813962-C-T

85062198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron_variant, undefined
orthologous variants: 145813958-T-C

85062258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: intron variant
orthologous variants: 145813898-A-G

85062350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 145813804-C-T

85062376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 145813780-C-G

85062565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145813586-G-A

85062565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145813586-G-T

85062571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 145813585-T-A

http://identifiers.org/hco/1/GRCh38#85062707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145813441-A-C

85062710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145813438-G-T

85062912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145813304-A-G

http://identifiers.org/hco/1/GRCh38#85062964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145813268-A-C

85071114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809948-T-A

85071274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809680-C-G

85071318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809658-A-T

85071335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809641-T-C

85071433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809577-G-T

85071582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809397-C-G

85071812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809066-G-A

85071812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809066-G-T

85071827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809051-A-G

http://identifiers.org/hco/1/GRCh38#85071829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145809049-C-A

85071829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809049-C-T

85071839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809044-T-A

85071839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809044-T-C

85071839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809044-T-G

85071847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809036-A-G

85071847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809036-A-T

85071862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809021-G-A

85071862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809021-G-T

85071894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145809003-A-G

85071973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145808929-G-A

85071973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145808929-G-C

85071973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145808929-G-T

85072021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145808853-C-T

85072077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145808803-T-C

85072124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145808751-A-G

http://identifiers.org/hco/1/GRCh38#85072997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145808538-A-C

85072998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145808537-A-G

85073001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145808534-G-A

85073001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145808534-G-T

85073232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145808316-A-G

85073333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145806697-T-C

85073392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145806651-A-G

85078537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145806477-A-G

http://identifiers.org/hco/1/GRCh38#85081121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145803175-A-C

85081121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145803175-A-G

85081314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145802995-G-A

85081314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145802995-G-T

http://identifiers.org/hco/1/GRCh38#85081477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145802835-C-A

http://identifiers.org/hco/1/GRCh38#85081556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145802778-A-C

85081556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145802778-A-G

85082330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145801130-T-G

http://identifiers.org/hco/1/GRCh38#85082414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145801046-C-A

85082414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145801046-C-T

85082425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145801035-T-C

85084469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145800205-G-A

85084469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145800205-G-T

85084557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 145800126-A-G

http://identifiers.org/hco/1/GRCh38#85084575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145800108-A-C

85084575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 145800108-A-G

85084603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145800080-T-C

85084603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145800080-T-G

http://identifiers.org/hco/1/GRCh38#85084618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145800065-C-A

85084618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145800065-C-T

85084674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 145800009-A-G

85084706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145799977-T-C

http://identifiers.org/hco/1/GRCh38#85084714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145799969-A-C

85084714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145799969-A-G

85084714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145799969-A-T

85084717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145799966-T-C

http://identifiers.org/hco/1/GRCh38#85084729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145799954-C-A

85084729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145799954-C-G

85084803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145799879-T-G

85084890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145799759-G-A

85085303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145799292-C-G

85085364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145799226-T-C

85085707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145798944-T-C

85085728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145798925-A-G

http://identifiers.org/hco/1/GRCh38#85085757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145798896-C-A

http://identifiers.org/hco/1/GRCh38#85085762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145798891-C-A

85085762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145798891-C-T

85085768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145798888-A-G

85085774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145798882-A-G

85085775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145798881-T-A

85085859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145798793-G-A

85085903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145798749-A-G

85085948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145798704-A-G

85086069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145798608-T-A

85086220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145798532-G-A

85086220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145798532-G-C

85086227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145798525-G-A

85086246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145798511-T-C

85088925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145797635-A-G

85088993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145797567-T-C

85089192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145797366-C-T

85089515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145797065-T-C

85089723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145796901-A-G

85089981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145788960-T-A

85089981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145788960-T-C

85089981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145788960-T-G

85089986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145788953-T-A

85089986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145788953-T-G

http://identifiers.org/hco/1/GRCh38#85090014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145788929-C-A

85090014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145788929-C-T

85090023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145788920-A-G

http://identifiers.org/hco/1/GRCh38#85090047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145788896-C-A

85090047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145788896-C-T

85090085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145788858-T-C

85090109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 145788835-A-G

85090187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 145788757-A-G

http://identifiers.org/hco/1/GRCh38#85090218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145788726-C-A

85091705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145787318-A-G

85093400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145787223-A-T

85093422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145787201-A-G

85093495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145787128-A-T

85093520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145787103-T-G

85093555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145787068-G-A

85093555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 145787068-G-T

85093668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145786966-G-T

85093711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145786945-A-G

85093712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145786944-T-C

85093790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 145786871-T-A

85093790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 145786871-T-C

85093800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 145786861-T-C

85093895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 145786716-G-A

85093895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 145786716-G-T

85093896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 145786715-A-G

85094362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 145786284-G-A

85094362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 145786284-G-C

http://identifiers.org/hco/1/GRCh38#85094369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145786277-C-A

http://identifiers.org/hco/1/GRCh38#85094578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145786073-A-C

85094578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145786073-A-G

85094594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145786057-A-G

http://identifiers.org/hco/1/GRCh38#85094620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145786031-C-A

85094725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145785503-A-G

85095736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145776666-G-A

85095787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145776615-G-T

http://identifiers.org/hco/1/GRCh38#85095814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145776591-C-A

85095814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145776591-C-T

85095817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145776588-A-T

85095904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145776528-T-C

85096009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145776423-A-G

85096009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145776423-A-T

85096012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145776420-A-G

85096087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145776360-G-T

85096115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145776330-T-A

85096123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145776322-A-G

85096149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145776296-A-T

85096196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145776246-A-G

http://identifiers.org/hco/1/GRCh38#85096256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145776191-C-A

85096323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145775972-A-G

85096404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145775890-A-G

85096454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145775854-G-A

85096571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145775823-T-C

85096597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145775793-A-G

85096597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145775793-A-T

85096619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145775773-T-C

85096762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145775405-G-A

85096854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145775310-A-G

85097020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145775148-A-G

85097023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145775145-G-T

85097187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145774994-G-A

85097418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145774768-A-T

85097437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145774749-A-T

85097631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145774509-T-G

http://identifiers.org/hco/1/GRCh38#85097661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145774479-C-A

85097661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145774479-C-G

85097661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145774479-C-T

http://identifiers.org/hco/1/GRCh38#85097678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145774457-C-A

85097726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145774408-G-A

85097726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145774408-G-T

85097751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145774380-G-A

85097751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145774380-G-C

85097751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145774380-G-T

http://identifiers.org/hco/1/GRCh38#85097795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145774343-A-C

85097795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145774343-A-T

85097919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145774214-T-A

85098359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145772842-A-G

http://identifiers.org/hco/1/GRCh38#85098430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145772773-A-C

85098430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145772773-A-T

http://identifiers.org/hco/1/GRCh38#85098437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145772766-A-C

85098437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145772766-A-T

85103565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145771598-A-G

85103979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145771518-C-T

http://identifiers.org/hco/1/GRCh38#85104419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145771184-C-A

85104419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145771184-C-T

http://identifiers.org/hco/1/GRCh38#85104429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145771171-C-A

85104429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145771171-C-G

85104560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145771121-G-A

85104587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145771094-T-G

85104681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145770995-T-C

85104818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145770523-G-A

85104818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145770523-G-C

85107893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145769359-T-C

85107893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145769359-T-G

85107974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145769300-G-T

85107982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145769292-G-T

85108073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145769195-A-G

85108151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145769060-G-A

85108151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145769060-G-C

85108151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145769060-G-T

85108181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145769030-A-G

85108227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145768995-T-G

85109887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145768243-G-A

http://identifiers.org/hco/1/GRCh38#85109899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145768231-C-A

85109912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145768221-G-A

85109912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145768221-G-T

85109913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145768220-G-T

85109920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145768213-G-A

85109920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145768213-G-T

85109942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145768194-G-A

85109942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145768194-G-T

85109943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145768193-T-G

85109994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145768138-A-T

85110005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145768127-C-T

http://identifiers.org/hco/1/GRCh38#85110771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145766771-C-A

85110811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145766731-A-G

85114765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145764183-C-T

85115200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145762679-G-A

85117247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145762111-T-A

85117323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145761791-C-T

85117336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145761778-A-G

85117512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145761647-G-A

85117633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145761566-A-G

85117815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145761384-A-G

85117874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145761325-T-C

85117894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145761306-T-C

85117894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145761306-T-G

85117908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145761299-A-G

http://identifiers.org/hco/1/GRCh38#85117919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145761289-C-A

85117919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145761289-C-T

http://identifiers.org/hco/1/GRCh38#85117964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145761265-A-C

85117964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145761265-A-G

http://identifiers.org/hco/1/GRCh38#85118015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145761213-A-C

85118030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145761198-A-G

85121421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145760676-T-C

85121615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145760491-T-C

85121826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145760295-G-T

85121849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145760273-G-A

85122937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145754971-G-A

http://identifiers.org/hco/1/GRCh38#85123110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145754798-C-A

85123425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145754498-A-T

85123713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145754251-G-A

http://identifiers.org/hco/1/GRCh38#85124111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145753989-A-C

85124111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145753989-A-G

http://identifiers.org/hco/1/GRCh38#85124260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145753840-C-A

85124308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145753796-C-T

http://identifiers.org/hco/1/GRCh38#85124317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145753787-C-A

85124373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145753732-G-T

85124470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145753638-G-A

85124535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145753565-T-A

85125061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145753408-G-C

85125063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145753406-G-A

85125063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145753406-G-C

85126611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145752364-G-C

85126761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145752216-G-A

85126761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145752216-G-T

http://identifiers.org/hco/1/GRCh38#85126865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145752126-C-A

85126865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145752126-C-G

85126865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145752126-C-T

85127063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145751939-T-C

85127174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145751842-T-G

85127550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145751392-A-G

85127734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145751202-G-A

http://identifiers.org/hco/1/GRCh38#85128455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145750915-C-A

85128455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145750915-C-G

85128482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145750890-G-A

85128558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145750830-G-A

85128558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145750830-G-T

85128565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145750823-A-T

http://identifiers.org/hco/1/GRCh38#85128582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145750801-C-A

85128582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145750801-C-T

85128610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145750773-T-C

http://identifiers.org/hco/1/GRCh38#85128635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145750747-A-C

85128661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145750721-T-C

85128682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145750699-C-T

85128684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145750697-T-C

85128746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145750624-A-G

85128746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145750624-A-T

85128771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 145750599-G-A

85128846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145750536-G-A

85128851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145750531-G-A

85128951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145749862-G-T

85129141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145749723-G-A

85129230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145749649-C-T

85129271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145749607-T-A

85129284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145749590-G-A

85129341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145749518-A-G

85129427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145749433-A-G

http://identifiers.org/hco/1/GRCh38#85129497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145749360-C-A

85129501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145749356-G-C

85129528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145749280-G-C

85129601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145749211-G-T

http://identifiers.org/hco/1/GRCh38#85129739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145749038-A-C

85129872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145748846-G-A

85129925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145748686-G-A

85129925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145748686-G-C

http://identifiers.org/hco/1/GRCh38#85129940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145748671-C-A

85129940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145748671-C-G

85129953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145748644-T-C

85130184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145748404-C-T

85130228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145748281-G-C

85130228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145748281-G-T

85130270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145748152-T-C

85130270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145748152-T-G

85130532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145747902-T-G

85130646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145747792-A-G

85130864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145747668-C-T

85130895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145747637-T-G

85131036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145747514-C-G

85131135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145747411-G-A

http://identifiers.org/hco/1/GRCh38#85131528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145747350-C-A

85131586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145747288-G-T

85131675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145747198-A-G

85132612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145746812-G-A

85132612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145746812-G-T

http://identifiers.org/hco/1/GRCh38#85132714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145746715-C-A

85132714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145746715-C-G

85132714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145746715-C-T

http://identifiers.org/hco/1/GRCh38#85132725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145746713-C-A

85132725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145746713-C-T

http://identifiers.org/hco/1/GRCh38#85132734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145746704-A-C

85132734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 145746704-A-T

http://identifiers.org/hco/1/GRCh38#85132794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145746644-C-A

85132876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145746573-G-A

85132943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145746506-T-C

85132948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 145746501-C-T

85132992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 145746457-G-T

http://identifiers.org/hco/1/GRCh38#85133066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30711
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145746360-C-A