84124814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87074526-T-C

84124848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87074586-A-G

84125118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87074817-C-T

84125285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87074984-A-G

84126234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075459-T-A

84126234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075459-T-C

84126234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075459-T-G

84126252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075477-A-G

84126252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075477-A-T

84126271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075495-G-A

84126271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075495-G-T

84126282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075503-A-T

84126327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075548-G-A

84126327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075548-G-T

http://identifiers.org/hco/6/GRCh38#84126334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87075582-A-C

84126334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075582-A-T

84126337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075585-A-G

84126341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075589-A-G

84126347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075595-T-C

84126348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075596-A-G

84126546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87075790-T-C

84126615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87075862-G-A

84127095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87076287-T-A

84127095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87076287-T-G

84127377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87076623-G-T

84138182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87079206-C-T

84138273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87079299-A-G

84138758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87079993-A-T

http://identifiers.org/hco/6/GRCh38#84138856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87080092-C-A

84138856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87080092-C-T

84138867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87080103-C-T

84139544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 87080749-A-G

84139803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87081209-T-C

84139837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87081235-C-T

84140176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87081487-G-A

84140176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87081487-G-T

84140243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87081523-C-T

84140249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87081529-C-T

84140289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87081569-T-C

84146584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87081927-G-A

84146584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87081927-G-T

84146640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87081989-T-C

84146859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87082287-A-G

84148856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87083124-C-T

84149092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87083329-A-T

84149114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87083352-T-C

84149456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87083658-G-C

84149456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87083658-G-T

84149673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87083862-T-C

http://identifiers.org/hco/6/GRCh38#84149712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87083901-C-A

84149712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87083901-C-T

http://identifiers.org/hco/6/GRCh38#84149748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87083933-A-C

84149748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87083933-A-T

84149757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87083942-T-C

84149758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87083943-T-G

84149800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87083963-G-T

84149803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87083966-A-G

84150218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87084116-A-G

http://identifiers.org/hco/6/GRCh38#84150918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87084665-A-C

84151002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87084727-T-C

84151047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87084770-C-T

84151159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87084883-T-C

84152451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87085604-G-A

84152451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87085604-G-T

84152522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87085672-T-C

84152654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 87085803-G-A

84152654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87085803-G-T

84152664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87085813-T-C

84152664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87085813-T-G

84152745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87085894-A-G

84152784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87085924-C-T

84152895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87086035-T-C

84152928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87086068-A-G

84152937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87086077-T-C

http://identifiers.org/hco/6/GRCh38#84152940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87086080-C-A

84152940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87086080-C-T

84152983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87086123-T-C

84153118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87086261-T-A

84153118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87086261-T-C

84153190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87086347-G-A

84153190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87086347-G-C

84153190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87086347-G-T

84154888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87088523-C-T

84154912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87088543-A-T

http://identifiers.org/hco/6/GRCh38#84154913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87088544-C-A

84154913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87088544-C-T

84154970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87088604-C-T

84155144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87088768-G-A

http://identifiers.org/hco/6/GRCh38#84155244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87088854-C-A

84155244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87088854-C-T

84155388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87088986-C-T

84155553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87089160-A-G

http://identifiers.org/hco/6/GRCh38#84158006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87089988-A-C

84158305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87090267-T-C

84158361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87090321-T-C

84158387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87090347-C-T

84158576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87090544-T-A

84158669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87090642-T-A

84158978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87090944-G-A

http://identifiers.org/hco/6/GRCh38#84159016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87090982-C-A

84159016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87090982-C-T

84159292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091229-G-T

84159872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091848-G-A

84159874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091850-G-A

84159909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091885-T-C

84159971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87091948-G-C

84160071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87092037-T-C

84160299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87092249-T-G

84160348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87092295-G-T

84160355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87092302-A-G

84160735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87092781-A-G

84160783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87092816-G-A

84160783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87092816-G-T

http://identifiers.org/hco/6/GRCh38#84161027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87093070-A-C

http://identifiers.org/hco/6/GRCh38#84161065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87093092-C-A

84161065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87093092-C-T

84161145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87093152-T-C

http://identifiers.org/hco/6/GRCh38#84161163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87093170-A-C

84161338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87093296-T-C

84161338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87093296-T-G

84161346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87093304-T-A

http://identifiers.org/hco/6/GRCh38#84161610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87093509-A-C

84161686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87093584-C-T

84161794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87093758-T-G

84161839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87093803-T-C

84161848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87093812-C-T

84161936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87093900-T-C

84161941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87093905-G-A

84161941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87093905-G-C

84161941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87093905-G-T

84162053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87094009-A-G

84162545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87094399-T-G

84162559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87094423-T-C

84162559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87094423-T-G

84162801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87094630-G-C

84163077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87094846-A-G

84163282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87095042-A-G

84163282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87095042-A-T

84163370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87095134-T-A

84163597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87095370-C-T

84165800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87097299-G-C

84165825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87097324-T-C

84165831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87097330-C-T

84166001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87097482-T-C

84169031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87098870-G-A

84169177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87098993-T-G

84169289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099079-T-A

84169303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099096-T-A

84169303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099096-T-C

84169303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099096-T-G

http://identifiers.org/hco/6/GRCh38#84169334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87099127-C-A

84169334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87099127-C-T

http://identifiers.org/hco/6/GRCh38#84169413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87099206-C-A

84169413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87099206-C-T

84169462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099241-T-C

http://identifiers.org/hco/6/GRCh38#84169502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87099280-C-A

84169502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099280-C-T

84169523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099285-T-C

84169544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099302-G-A

84169544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099302-G-T

http://identifiers.org/hco/6/GRCh38#84169546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87099304-A-C

84169546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099304-A-T

84169664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099394-T-C

84169767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099487-G-C

84169954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099646-C-G

84170014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87099702-C-T

84171016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87100028-G-A

84171040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87100055-T-C

http://identifiers.org/hco/6/GRCh38#84171068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87100086-C-A

http://identifiers.org/hco/6/GRCh38#84171100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87100105-C-A

84171100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87100105-C-T

84171102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87100107-C-G

http://identifiers.org/hco/6/GRCh38#84171124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87100129-C-A

84171294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87100288-T-C

84171352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87100346-A-G

http://identifiers.org/hco/6/GRCh38#84171837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87100777-C-A

84171837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87100777-C-G

84171837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87100777-C-T

84174029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102483-T-C

84174170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87102626-T-C

84174199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102655-T-C

84174225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102681-G-A

84174225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102681-G-T

84174228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102684-A-T

84174272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102711-T-G

84174273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102712-T-C

http://identifiers.org/hco/6/GRCh38#84174278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87102717-C-A

84174278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102717-C-G

84174278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102717-C-T

http://identifiers.org/hco/6/GRCh38#84174302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87102739-C-A

84174302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102739-C-T

84174498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87102921-G-A

84174693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103112-A-T

http://identifiers.org/hco/6/GRCh38#84174712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87103136-C-A

84174712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103136-C-G

84174761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87103185-T-A

84174761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87103185-T-C

84174761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87103185-T-G

84174781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87103205-T-C

84174814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87103238-T-C

84174830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87103254-G-A

84174830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 87103254-G-C

84174830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 87103254-G-T

84174872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87103296-C-T

84174975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103400-T-C

84175051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103472-T-C

84175059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103480-T-C

84175059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103480-T-G

84175064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87103485-T-C

84175196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104074-T-C

84175296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87104176-G-A

84175296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87104176-G-T

http://identifiers.org/hco/6/GRCh38#84175307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87104187-C-A

84175307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87104187-C-G

84175307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87104187-C-T

84175388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104291-A-G

84175390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104293-G-C

84175390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104293-G-T

84175531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104405-T-C

http://identifiers.org/hco/6/GRCh38#84175770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87104616-C-A

84175792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104636-A-G

84175857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104690-T-C

84175923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104758-T-C

84176031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87104868-T-C

84176191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105030-T-C

84176296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105114-C-T

84176310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105130-T-C

84182793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87105837-C-T

84183117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87106144-T-C

84183297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87106293-C-T

84185037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87107559-T-C

84185080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87107602-G-A

84185102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87107629-T-C

http://identifiers.org/hco/6/GRCh38#84185135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87107661-C-A

84185135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87107661-C-T

84185142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87107668-G-T

84185228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87107773-T-G

http://identifiers.org/hco/6/GRCh38#84185454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87107999-C-A

84185454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87107999-C-T

84185496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108041-T-A

84185496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108041-T-C

84185497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108042-A-G

84185497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108042-A-T

84185516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108060-T-A

84185516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108060-T-C

84185566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108107-G-A

84185602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108137-A-G

84185880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108680-C-G

84186029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108828-T-C

84186029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108828-T-G

84186039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87108838-A-G

84186466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87109323-T-C

http://identifiers.org/hco/6/GRCh38#84186563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: http://identifiers.org/mco/9/GRCm39#87109420-C-A

http://identifiers.org/hco/6/GRCh38#84186610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87109467-C-A

84186610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87109467-C-T

84186731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87109567-G-A

84186731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87109567-G-C

84186731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87109567-G-T

84186804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87109665-A-G

84187272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110335-T-C

84187302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110363-G-C

84187471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110495-C-T

84187480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110504-T-C

84187483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110507-C-T

84187497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110521-T-C

84187507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110531-T-C

84187718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110703-C-T

84187814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110793-A-G

84187861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110856-T-C

84187889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110884-G-A

84187969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87110947-C-T

http://identifiers.org/hco/6/GRCh38#84192339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87112255-C-A

84192339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112255-C-G

84192383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112281-G-A

84192470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112340-G-A

84192503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112369-G-A

84192516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112381-T-G

84192644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87112500-T-C

84192794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112632-G-T

84192909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87112739-G-A

http://identifiers.org/hco/6/GRCh38#84192960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87112793-C-A

84192992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87112823-T-C

http://identifiers.org/hco/6/GRCh38#84193209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#87113032-C-A

84193298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87113117-A-G

84193507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113291-G-A

84193507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113291-G-C

84193516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113304-G-T

84193519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113307-T-C

http://identifiers.org/hco/6/GRCh38#84193587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#87113372-A-C

84193587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87113372-A-G

84193606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87113428-T-C

http://identifiers.org/hco/6/GRCh38#84193639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87113461-C-A

84193664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87113486-T-C

84193733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113558-G-A

84193733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113558-G-T

http://identifiers.org/hco/6/GRCh38#84193742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#87113567-A-C

84193742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87113567-A-G

http://identifiers.org/hco/6/GRCh38#84193782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87113611-C-A

http://identifiers.org/hco/6/GRCh38#84193795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87113623-A-C

84193795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113623-A-G

84193833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113660-T-A

84193833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113660-T-C

http://identifiers.org/hco/6/GRCh38#84193934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87113727-C-A

84193934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113727-C-T

84194782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113915-T-C

84194782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113915-T-G

84194854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113973-T-C

84194854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87113973-T-G

84194902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87114050-T-C

84194967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87114115-G-A

84194986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87114134-G-C

84194986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87114134-G-T

84195153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87114284-T-A

http://identifiers.org/hco/6/GRCh38#84195220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87114370-C-A

84195224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87114374-G-A

84195224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87114374-G-T

84195555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87114673-G-A

84195622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87114737-A-T

84195626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87114741-T-C

84196570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87116187-G-A

84197410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87116861-C-G

84197469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87116921-T-C

http://identifiers.org/hco/6/GRCh38#84198060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87117123-C-A

84198655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87117766-T-C

84198663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87117774-C-T

84198713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87117841-T-C

84198716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87117844-T-A

84198947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87118052-G-A

84199200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87118274-C-T

84199287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87118355-G-A

84200472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87119702-T-C

84200823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87119920-T-C

84200834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87119931-G-T

84201503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87120187-T-C

84201596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87120290-T-A

84201596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87120290-T-C

84201596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87120290-T-G

http://identifiers.org/hco/6/GRCh38#84201667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87120355-A-C

84201846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87120507-A-G

http://identifiers.org/hco/6/GRCh38#84201905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87120554-C-A

84202032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87120664-A-G

84202780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87121102-G-C

84202917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87121235-G-A

84203850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87121748-G-T

http://identifiers.org/hco/6/GRCh38#84203928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87121819-C-A

84203928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87121819-C-T

http://identifiers.org/hco/6/GRCh38#84203929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87121820-C-A

84203935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87121826-G-C

84203935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87121826-G-T

84203972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87121861-T-C

84204013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87121900-A-G

84204013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87121900-A-T

84204028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87121915-G-C

84204028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87121915-G-T

84204036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87121923-T-C

84204056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87121943-T-A

84204056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87121943-T-C

84204064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87121951-C-T

http://identifiers.org/hco/6/GRCh38#84204122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87122009-C-A

http://identifiers.org/hco/6/GRCh38#84204146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87122030-C-A

84204167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87122051-T-A

84204167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87122051-T-C

http://identifiers.org/hco/6/GRCh38#84204181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87122065-A-C

84204181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87122065-A-T

84204198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87122079-T-C

84204198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87122079-T-G

84204205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87122086-T-C

84208094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87122197-C-G

84209814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87122967-C-T

84210132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87123123-C-G

84210485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87123461-T-C

84210489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87123464-C-T

84210556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87123519-G-A

84210556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87123519-G-C

84210570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87123530-G-T

84210633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87123587-T-C

84210635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87123589-A-G

84210832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87123781-T-C

84210925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87123892-G-A

84210927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87123894-T-C

84211116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87124037-G-A

84211213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87124119-T-A

84211289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87124160-G-A

84211310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87124178-T-C

84211372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87124222-C-T

84211393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87124255-T-A

84211393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87124255-T-C

84211452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87124309-G-A

84211452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87124309-G-T

84211475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87124320-C-T

84211476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87124321-G-A

84211489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87124333-T-C

84211505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87124345-T-A

84211567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87124436-T-A

84212220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87125148-C-G

84212254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87125181-A-T

http://identifiers.org/hco/6/GRCh38#84212337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87125240-C-A

84212399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87125296-A-G

84212496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87125382-T-C

84212590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87125477-C-T

http://identifiers.org/hco/6/GRCh38#84212812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87126201-C-A

84212812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87126201-C-G

84212823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87126212-A-T

http://identifiers.org/hco/6/GRCh38#84212845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87126242-C-A

84212855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87126252-A-G

http://identifiers.org/hco/6/GRCh38#84212909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87126305-C-A

84212909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87126305-C-G

84212925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87126321-A-G

84212970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87126344-A-G

http://identifiers.org/hco/6/GRCh38#84213011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87126385-C-A

84213011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87126385-C-G

84213011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87126385-C-T

84213016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87126390-G-A

84213016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87126390-G-T

84213044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87126415-A-G

84213044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87126415-A-T

http://identifiers.org/hco/6/GRCh38#84213079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87126447-C-A

84213079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87126447-C-G

84213079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87126447-C-T

84213101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87126479-T-A

http://identifiers.org/hco/6/GRCh38#84213122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87126498-C-A

84213122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87126498-C-T

84213238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87126612-A-G

http://identifiers.org/hco/6/GRCh38#84213461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87126843-A-C

84214508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87127290-G-A

84214728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87127480-A-G

84214853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87127594-G-A

84214979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87127699-A-G

84215125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87127850-A-G

84215135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87127860-T-C

84215160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87127882-A-T

http://identifiers.org/hco/6/GRCh38#84215168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87127890-A-C

84215168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87127890-A-T

http://identifiers.org/hco/6/GRCh38#84215224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87128040-C-A

84215224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87128040-C-T

http://identifiers.org/hco/6/GRCh38#84215232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87128092-C-A

84215232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87128092-C-T

84215270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87128191-A-G

84215304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87128224-T-A

84215305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87128225-A-G

84215442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87128362-G-A

84215442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87128362-G-T

84215464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 87128384-T-C

http://identifiers.org/hco/6/GRCh38#84215501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87128424-C-A

84215501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87128424-C-T

84215522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87128440-T-G

84215618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87128507-T-A

84215654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87128545-C-G

84215654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87128545-C-T

http://identifiers.org/hco/6/GRCh38#84215730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87128628-C-A

84215730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87128628-C-T

84215743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87128640-A-G

http://identifiers.org/hco/6/GRCh38#84215755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87128652-C-A

84215755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87128652-C-T

http://identifiers.org/hco/6/GRCh38#84215756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87128653-A-C

84215756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87128653-A-G

84215831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87128724-T-C

84215855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87128748-T-A

84215855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87128748-T-C

84215920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 87128813-G-A

84215920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 87128813-G-T

84215949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87128858-A-T

84216028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87128937-T-A

84216110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87129018-T-C

http://identifiers.org/hco/6/GRCh38#84216144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87129056-C-A

84216294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87129084-T-C

http://identifiers.org/hco/6/GRCh38#84216434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87129205-A-C

84216524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87129274-G-C

84216524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87129274-G-T

84216527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87129279-C-T

84219113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87129780-A-G

84219114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87129781-T-C

84219119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87129790-A-G

84219141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87129812-G-A

84219141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87129812-G-T

84219164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87129833-G-A

84219164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87129833-G-T

84219188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 87129857-T-C

84219206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 87129873-T-C

84220690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87130130-G-C

84220901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87130262-T-C

84220917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87130277-T-C

84220947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87130307-A-G

84220978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87130338-A-T

84220990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87130350-A-G

84221100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87130471-A-G

84221100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87130471-A-T

84221113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: 87130484-A-T

84221163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87130543-A-G

84221174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87130554-G-A

84221174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87130554-G-T

84221187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87130567-G-T

http://identifiers.org/hco/6/GRCh38#84221219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87130599-A-C

84221219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87130599-A-T

84221252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87130633-T-C

84221293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87130662-T-C

84221324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87130692-C-T

84221640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87131323-A-G

84221719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87131405-A-G

84221757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87131437-T-C

84221866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87131547-C-T

84221891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87131572-C-G

84221925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87131618-C-G

84221925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87131618-C-T

84221979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87131668-C-G

84222955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87134786-T-C

84222975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87134806-T-G

84226194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87135818-G-A

http://identifiers.org/hco/6/GRCh38#84226209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87135836-C-A

84226209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87135836-C-G

84226210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87135837-A-G

http://identifiers.org/hco/6/GRCh38#84226214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87135846-C-A

84226215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87135847-T-C

84226235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87135870-A-G

84226247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87135882-T-A

84226247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87135882-T-C

84226249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87135884-G-T

84226315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87135957-G-T

http://identifiers.org/hco/6/GRCh38#84226414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87136062-C-A

84226414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87136062-C-T

84226531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87136204-T-C

84226531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87136204-T-G

84226547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87136221-T-C

84226551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87136225-T-C

84226551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87136225-T-G

http://identifiers.org/hco/6/GRCh38#84226553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87136227-C-A

84226558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87136232-T-A

http://identifiers.org/hco/6/GRCh38#84226585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#87136259-A-C

84226585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87136259-A-G

84226705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87136376-T-A

84226705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87136376-T-C

84226856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87136529-C-G

84227058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87136833-T-C

84227234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87137010-G-A

84227274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87137033-G-A

84227274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87137033-G-C

84227433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87137186-G-T

84227473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87137216-G-A

84227565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87137304-C-T

84227583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21107
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87137323-T-C