70043844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425705-G-A

70043844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425705-G-T

70043872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425678-T-C

http://identifiers.org/hco/9/GRCh38#70043917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23425632-C-A

70043917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425632-C-T

http://identifiers.org/hco/9/GRCh38#70043927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23425622-C-A

70043927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425622-C-T

70043935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425613-A-G

70043936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425612-G-A

70043936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425612-G-T

http://identifiers.org/hco/9/GRCh38#70043943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23425605-C-A

70043943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425605-C-G

70043944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425604-G-A

70043944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425604-G-T

70043952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 23425597-A-T

70043960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425589-C-T

70043972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425577-G-A

70043972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425577-G-T

http://identifiers.org/hco/9/GRCh38#70044138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23425473-C-A

70044173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425445-T-A

70044173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425445-T-C

70044175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425443-G-C

70044251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425369-A-T

70044256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425364-C-T

70044488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23425140-T-C

http://identifiers.org/hco/9/GRCh38#70044578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#23425061-C-A

70044578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 23425061-C-T

70044596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23425043-C-T

70044597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 23425042-C-G

70044597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 23425042-C-T

70044662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23424977-T-C

http://identifiers.org/hco/9/GRCh38#70044709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23424930-C-A

70044709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424930-C-G

70044709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424930-C-T

70044723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424916-G-A

http://identifiers.org/hco/9/GRCh38#70044938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23424715-C-A

70044938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424715-C-T

70045142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424537-T-A

70045142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424537-T-C

70045205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424479-T-G

70045498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424196-C-T

70045633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424072-C-T

70045638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424067-C-T

70046062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23423673-G-A

70046079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23423656-G-A

70046079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23423656-G-T

70046092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23423644-G-C

70046109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23423626-G-A

70046404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23423281-C-G

http://identifiers.org/hco/9/GRCh38#70046592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23423010-A-C

70046833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422775-G-A

70047792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422319-G-A

70047811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422305-T-C

70048251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422028-G-A

70048719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421897-C-T

70048828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421800-C-G

70048917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421729-T-G

http://identifiers.org/hco/9/GRCh38#70049010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23421657-C-A

http://identifiers.org/hco/9/GRCh38#70049281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23421415-A-C

70049397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421305-T-A

70049397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421305-T-C

70049462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421257-G-A

70049498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421239-T-C

http://identifiers.org/hco/9/GRCh38#70050068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23420680-A-C

70050085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420663-A-G

70050090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420658-T-C

70050148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420601-A-G

http://identifiers.org/hco/9/GRCh38#70050580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23419478-A-C

70050709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23419354-T-C

70050753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23419302-T-C

70050907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23419149-A-G

http://identifiers.org/hco/9/GRCh38#70051187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23418888-A-C

70051355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23418738-G-A

70051355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23418738-G-T

70051499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23418578-T-C

70051550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23418099-G-T

70051562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23418086-T-A

70051565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23418083-A-G

70051686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417961-A-T

70051730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417921-T-A

70051730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417921-T-C

70052036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417583-C-G

70052072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417547-A-G

http://identifiers.org/hco/9/GRCh38#70052182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23417436-C-A

http://identifiers.org/hco/9/GRCh38#70052196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23417422-A-C

70052241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417363-T-C

70052326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417214-C-G

70052739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23416563-A-T

70053121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23416211-A-G

70053311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23416015-T-A

70053344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415983-A-T

70053485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415849-C-T

70053493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415841-C-T

70053502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415832-G-T

70053774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415559-G-A

70053842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415510-G-A

70054037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415337-T-C

70054113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415261-C-G

70054139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415235-C-T

70054196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413587-G-A

70054199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413584-A-G

http://identifiers.org/hco/9/GRCh38#70054200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23413583-C-A

70054200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413583-C-T

70054467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413233-G-T

70054596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23412979-G-T

70054615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23412961-G-A

http://identifiers.org/hco/9/GRCh38#70055302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23412697-A-C

70055498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23412561-C-T

70055509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23412551-T-C

http://identifiers.org/hco/9/GRCh38#70055662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23412387-A-C

70055843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23412189-C-G

http://identifiers.org/hco/9/GRCh38#70056182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23411851-A-C

70056615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23410871-G-A

70057334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23410679-C-G

http://identifiers.org/hco/9/GRCh38#70057471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23410535-C-A

http://identifiers.org/hco/9/GRCh38#70058233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23409855-A-C

70058243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409845-C-T

70058251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409837-G-A

70058306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409789-G-A

70058599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409521-G-A

70058620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409500-C-G

70058620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409500-C-T

70058800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409221-A-G

70058946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409086-T-C

70058987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409045-G-T

70059262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23408797-G-A

70059280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23408780-T-C

70059324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23408739-G-A

70059327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23408736-G-A

70059327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23408736-G-C

70059411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23408658-T-A

70059411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23408658-T-C

70061929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23406208-T-C

70062212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23405925-T-C

70062262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23405818-C-T

http://identifiers.org/hco/9/GRCh38#70062277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23405721-A-C

70062277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23405721-A-G

70062338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23405533-A-G

70062465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23405425-G-T

70064507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23400004-A-G

70064810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399748-C-T

70065341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399226-A-T

70065354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399213-G-T

70065391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399176-T-G

http://identifiers.org/hco/9/GRCh38#70065422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23399067-A-C

70065423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399043-G-C

70065463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23398996-C-T

70065505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23398957-T-C

70065579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23398882-C-T

70066133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397341-G-A

70066183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397297-A-G

70066186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397294-G-A

http://identifiers.org/hco/9/GRCh38#70066207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23397274-C-A

70066207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397274-C-G

70066207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397274-C-T

http://identifiers.org/hco/9/GRCh38#70066231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23397250-C-A

70066231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397250-C-T

70066327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397176-G-A

70066449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397093-C-T

70066560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23396996-T-A

70066560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23396996-T-C

70066606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23396949-C-T

70066745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23396859-G-A

70067189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23395859-T-C

70067319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23395735-T-G

70067596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23395469-C-G

70067657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23395423-G-T

70067860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23395249-T-A

70068020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23395089-T-C

70068127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23394988-G-A

70069071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23393235-G-C

70069170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23393166-A-G

70069333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23392976-C-T

70069473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23392883-C-T

70069705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23392500-G-T

70070198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391986-G-A

70070227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391957-C-T

70070264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391919-A-G

70070627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23390779-A-T

70070860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23390538-C-T

70070872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23390524-G-A

70070996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23390398-T-G

70071048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23390342-G-A

70071171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23390214-T-C

70071224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23390178-G-A

70071272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23390139-T-C

70071487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389778-C-T

70071537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389721-G-A

70071688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23389568-G-A

70071733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23389520-C-T

70071781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389475-G-T

http://identifiers.org/hco/9/GRCh38#70071823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23389447-C-A

70071831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389439-T-C

70071844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389428-G-A

70071844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389428-G-T

70072043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389244-T-A

70072370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388824-G-A

70072492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388728-T-C

70072558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388660-A-G

70072679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388574-G-A

70072695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388557-A-G

70073586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23387970-A-G

http://identifiers.org/hco/9/GRCh38#70073720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23387387-C-A

70073823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23387290-T-C

70073890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23387229-C-G

70073890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23387229-C-T

70074650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23383986-C-G

70074719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23383918-G-A

70074719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23383918-G-C

70074848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23383776-C-T

70074850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23383774-T-C

70075631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23383041-A-G

70075994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23382882-T-A

70076068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23382827-C-T

70076529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23382365-A-T

70076625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23382292-C-G

70076825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23382078-T-C

70077070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23381861-G-A

70077166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23381766-C-T

70077279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23381219-C-T

70077770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23380790-A-G

70077798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23380762-T-C

70077963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23380345-G-A

70078115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23380229-G-A

http://identifiers.org/hco/9/GRCh38#70078816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23380005-A-C

70078826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379994-C-T

70078833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379987-A-G

70079046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379792-A-G

http://identifiers.org/hco/9/GRCh38#70079094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23379744-C-A

70079094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379744-C-G

70079098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379739-G-T

http://identifiers.org/hco/9/GRCh38#70079099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23379738-C-A

70079125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379712-C-T

70079161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379674-T-C

http://identifiers.org/hco/9/GRCh38#70079195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23379639-C-A

70079261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23379571-G-A

70079261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23379571-G-C

70079271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23379561-A-G

70079294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23379538-A-T

70079542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379296-G-A

70079542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379296-G-T

70079592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379247-T-C

70079737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379102-C-T

70079912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23378924-A-G

70080603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23378082-T-C

http://identifiers.org/hco/9/GRCh38#70081475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23377701-C-A

http://identifiers.org/hco/9/GRCh38#70081479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23377697-C-A

70081479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23377697-C-T

70081826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23377426-C-T

70081830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23377422-A-G

70081841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23377411-G-T

70081900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23377361-G-A

70081986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23377295-T-A

70081986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23377295-T-C

70082064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23377249-G-T

http://identifiers.org/hco/9/GRCh38#70082068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23377245-C-A

70082709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23376706-T-C

70082783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23376632-G-C

70082790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23376625-A-G

70082869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23376546-T-C

http://identifiers.org/hco/9/GRCh38#70082976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23376436-A-C

70083054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23376361-T-C

70083069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23376333-G-A

70083182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23376126-G-C

70083306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23376006-A-G

70083392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23375918-T-A

70083415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23375902-T-C

http://identifiers.org/hco/9/GRCh38#70083488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23375826-C-A

http://identifiers.org/hco/9/GRCh38#70083494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23375819-C-A

70083528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23375785-A-G

70083701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23375081-T-C

70083745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23375046-C-G

70083745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23375046-C-T

70083781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23375019-C-T

70083805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374995-T-C

http://identifiers.org/hco/9/GRCh38#70083826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23374975-C-A

70083826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374975-C-T

70083894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374904-T-C

70084101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374710-A-T

70084120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374689-T-G

70084583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374250-C-T

70084624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374209-A-G

70084720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374107-T-C

70084720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23374107-T-G

70084889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23373948-G-A

70084934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23373907-G-A

70085590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23373370-C-T

http://identifiers.org/hco/9/GRCh38#70085758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23373012-C-A

70086253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23372614-C-T

70086299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23372584-A-G

70086356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23372529-T-C

70086387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23372498-G-T

http://identifiers.org/hco/9/GRCh38#70086456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23372415-C-A

70086456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23372415-C-T

70086495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23372328-G-T

70086535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23372149-G-A

70086535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23372149-G-T

70086597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23372089-G-A

70086629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23372057-G-T

70086668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23372017-C-T

70086822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23371867-T-C

70086969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23371716-A-T

70087061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23371620-G-T

70087090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23371586-G-T

http://identifiers.org/hco/9/GRCh38#70087325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23371374-C-A

70087325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23371374-C-T

70087373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23371279-A-G

70087381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23371271-G-T

70087434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23371215-G-A

70087434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23371215-G-T

70087544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23371111-C-T

http://identifiers.org/hco/9/GRCh38#70088816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23370962-A-C

70089373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23370746-G-T

http://identifiers.org/hco/9/GRCh38#70089909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23370251-A-C

70089919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23370241-T-G

70089973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23370170-T-G

70090014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23370128-A-G

70090150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23370019-C-T

70090159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23370005-A-G

70091451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368674-T-C

70091464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368660-A-T

http://identifiers.org/hco/9/GRCh38#70091487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23368637-C-A

70091579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368548-A-T

70091709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368419-T-C

70091794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368342-A-G

http://identifiers.org/hco/9/GRCh38#70091934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23368230-A-C

70092113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23368074-A-G

http://identifiers.org/hco/9/GRCh38#70092138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23368052-C-A

70092261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23367950-G-A

http://identifiers.org/hco/9/GRCh38#70092327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23367893-C-A

70092327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23367893-C-T

70092438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23367830-G-T

http://identifiers.org/hco/9/GRCh38#70092531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23367759-C-A

70092586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23367704-G-A

70092586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23367704-G-T

http://identifiers.org/hco/9/GRCh38#70092677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23367631-C-A

70092998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23366675-T-G

70093137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23366543-C-T

70093692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23366149-A-T

http://identifiers.org/hco/9/GRCh38#70093715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23366132-A-C

70093715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23366132-A-G

70093762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23366075-G-A

70093943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23365921-T-C

70094052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23365814-T-C

70094052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23365814-T-G

70094084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23365784-G-A

70094084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23365784-G-T

70094182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23365693-T-C

70094282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23365615-T-C

70094418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23365463-T-G

70094437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23365444-G-T

70094491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23365388-T-C

70097467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23364814-C-T

70097475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23364806-T-C

70097499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23364782-G-A

70097499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23364782-G-T

http://identifiers.org/hco/9/GRCh38#70097811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23364481-A-C

70098185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23364151-A-G

70098283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23364077-C-T

70098395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23363990-T-G

70098542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23363787-C-T

70098600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23363730-T-C

70098739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23363527-G-T

70098961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23363113-A-T

70099956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23362021-C-T

70100067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23361979-T-A

70100084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23361962-G-A

70100124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23361919-T-C

70100317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23361712-C-T

70104142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23360982-C-T

http://identifiers.org/hco/9/GRCh38#70104147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23360977-A-C

70104267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23360872-T-A

70104381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23360751-T-C

70104974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23360215-T-C

70105254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23359982-G-A

70105423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23359813-G-A

70105531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23359726-A-G

70105684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23359581-G-T

http://identifiers.org/hco/9/GRCh38#70105834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23358929-C-A

70105834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23358929-C-T

70105905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23358865-C-T

70106036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23358762-G-C

70106239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23358668-G-C

http://identifiers.org/hco/9/GRCh38#70106410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23358116-C-A

70106418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23358108-C-T

70106593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357938-G-A

70106664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357869-G-A

70106718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357816-C-G

70106876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357688-G-A

70106924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357640-C-T

70106959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357600-A-G

70107003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357559-C-G

http://identifiers.org/hco/9/GRCh38#70107061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23357512-C-A

70107146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357434-C-T

70107161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357425-A-G

70107215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357371-G-C

70107251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357335-G-T

70107374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357208-G-A

70107412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23357173-A-G

http://identifiers.org/hco/9/GRCh38#70107832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23356776-A-C

70107846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23356762-G-A

http://identifiers.org/hco/9/GRCh38#70107963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23356646-C-A

70108218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 23356289-C-T

70108223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23356284-A-T

70108344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 23356163-G-A

70108344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 23356163-G-C

70108393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23356114-T-G

http://identifiers.org/hco/9/GRCh38#70108464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23356043-C-A

70108464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23356043-C-G

70108464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 23356043-C-T

70108474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23356033-A-G

70108474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 23356033-A-T

70108484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 23356023-T-C

http://identifiers.org/hco/9/GRCh38#70108615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23355696-C-A

70108615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23355696-C-T

70108668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23355650-G-A

70109073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23355288-T-C

70109091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23355271-T-C

70109234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23355140-G-A

70109234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23355140-G-C

70109234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23355140-G-T

70109237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23355137-A-G

70109244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23355130-G-A

70109244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23355130-G-T

70109269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23355104-T-C

70109427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23354954-G-T

70109441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23354939-G-A

70109441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23354939-G-T

http://identifiers.org/hco/9/GRCh38#70109445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23354935-A-C

70109445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23354935-A-G

http://identifiers.org/hco/9/GRCh38#70109476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23354910-C-A

70109685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23354744-A-T

70109855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23354581-G-A

70109855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23354581-G-T

70110145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23354270-A-G

http://identifiers.org/hco/9/GRCh38#70110302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23354097-C-A

70110936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353583-G-A

70111125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23353392-A-G

70111298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23353042-G-A

70111483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23352890-C-G

70111528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23352852-T-A

70111547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23352833-T-G

70112014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23352311-A-G

70112142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23352238-C-T

70112223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23352183-T-C

70112250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23352163-A-G

70112297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23352117-A-G

70112518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351905-T-A

http://identifiers.org/hco/9/GRCh38#70112846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23351566-C-A

70112846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351566-C-T

70112867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351545-G-A

70112867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351545-G-C

70112867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351545-G-T

70112913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351512-T-A

70112918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351507-G-C

70112918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351507-G-T

70112935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351489-G-C

70112972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351443-G-A

http://identifiers.org/hco/9/GRCh38#70112984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23351429-C-A

70112984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351429-C-T

70113094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23351318-C-G

70113260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351185-A-G

70113290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351155-G-A

70113384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351071-C-T

http://identifiers.org/hco/9/GRCh38#70113609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23350886-C-A

70113609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350886-C-G

70113618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350877-A-G

70113618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350877-A-T

70113623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350872-G-A

70113623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350872-G-T

70113667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350835-A-G

70113667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350835-A-T

70113670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350832-G-A

70113670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350832-G-T

70113707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350809-G-T

70113818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23350702-G-A

70113818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23350702-G-T

70113864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23350661-T-C

70113899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350626-G-C

70113899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350626-G-T

70113900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350625-C-T

70113934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350603-G-A

70113947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350590-G-T

70114023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350516-G-A

70114114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350426-C-T

70114248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350299-T-C

70114248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350299-T-G

70114346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350212-A-G

70114414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350155-G-C

70118292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23349610-C-T

70118295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23349607-T-A

70118395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23349511-A-G

http://identifiers.org/hco/9/GRCh38#70118446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23349461-C-A

70118446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23349461-C-G

70118446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23349461-C-T

http://identifiers.org/hco/9/GRCh38#70118693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23349218-C-A

70118693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23349218-C-T

http://identifiers.org/hco/9/GRCh38#70118836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23349125-A-C

70118999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23348970-A-G

70119117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23348889-T-C

70119427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23348557-A-G

70119529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23348457-A-G

70119541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23348445-T-C

70119549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23348437-C-T

70119655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23348319-A-T

70119859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23348120-C-T

70120008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23347977-C-T

70120021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23347964-C-T

70120026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23347962-T-C

70120744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23345771-C-T

70120861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23345653-G-A

70120909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23345613-G-A

70121315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23345225-C-T

70121344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23345203-G-A

70121550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23345021-C-G

70121550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23345021-C-T

70121612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23344856-T-C

70121742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23344666-G-C

70122151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23344291-A-G

70122521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23343832-G-C

70122855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23343453-C-G

70122855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23343453-C-T

70122941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23343387-G-C

70122951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23343377-G-T

70122993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23343335-G-T

70123024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23343302-A-G

70123309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23343043-C-T

70125202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23342678-C-T

70125394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341973-G-A

70125458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341912-C-G

70125458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341912-C-T

70125518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341859-G-T

70125562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341806-C-T

70125655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341757-A-G

70125770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341658-C-T

70125954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341497-G-A

70125959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341492-G-A

70126009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341447-G-A

70126009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341447-G-T

70126053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341427-T-A

70126053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341427-T-C

70126061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341419-G-T

70126065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341415-T-G

70126072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341408-A-G

http://identifiers.org/hco/9/GRCh38#70126084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23341396-C-A

70126084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341396-C-T

http://identifiers.org/hco/9/GRCh38#70126094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23341388-C-A

70126094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341388-C-T

http://identifiers.org/hco/9/GRCh38#70126101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23341381-C-A

70126101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341381-C-T

70126144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23341343-C-G

70126257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23341230-T-A

http://identifiers.org/hco/9/GRCh38#70126308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23341179-A-C

70126308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23341179-A-G

70126365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23341122-G-T

70127081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23339144-A-T

70127183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23339061-T-G

70127445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23338796-T-C

70127529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23338717-A-G

70127894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23338273-A-T

70130159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23337728-T-G

http://identifiers.org/hco/9/GRCh38#70131039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23337018-C-A

70131233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23336859-C-T

70131411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23336702-A-G

70131433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23336680-T-C

70131558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23336566-T-C

http://identifiers.org/hco/9/GRCh38#70131733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23336393-A-C

http://identifiers.org/hco/9/GRCh38#70131968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23336132-C-A

70131968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23336132-C-G

70132076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23336035-C-T

70132207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23335904-G-T

70132241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23335870-A-T

70134694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23334128-T-G

70134783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23334040-C-T

70134991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23333842-A-T

http://identifiers.org/hco/9/GRCh38#70135023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23333810-C-A

70135247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23333606-G-A

http://identifiers.org/hco/9/GRCh38#70135377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23333471-A-C

70135466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23333388-T-C

70136285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23332926-A-G

70136545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23332653-A-G

70136741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23332525-T-G

70137130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23332177-A-G

70137130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23332177-A-T

70137491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23331854-A-G

70137566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23331781-T-G

70137590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23331757-C-T

http://identifiers.org/hco/9/GRCh38#70137842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23331511-A-C

70137842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23331511-A-G

70138764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23331383-G-A

70138764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23331383-G-T

70138801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23331346-G-T

70138856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23331291-T-C

70139988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330941-A-T

70140109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330845-T-C

70140162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23330792-G-A

70140175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23330779-G-A

70140175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23330779-G-C

70140221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 23330733-T-C

70140343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330621-G-A

70140432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330542-G-A

70140432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330542-G-T

70140475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330499-C-T

70140526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330449-T-C

70141506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330347-T-C

70141519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330333-T-A

70141593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330253-C-T

http://identifiers.org/hco/9/GRCh38#70141616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23330229-A-C

70141677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330162-G-A

70141722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330117-T-A

70141762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330078-G-T

70141789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330068-A-G

70141790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330067-T-A

70141790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330067-T-C

70141812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330045-T-C

70141844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330013-T-C

70141855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23330002-T-C

http://identifiers.org/hco/9/GRCh38#70141905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23329958-A-C

70141933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23329936-A-G

70142276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23329662-C-T

70142342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23329621-A-G

70142377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23329592-T-C

70142622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23329356-G-C

70142891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23329113-C-T

http://identifiers.org/hco/9/GRCh38#70143414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23328585-C-A

70143417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23328582-A-G

70143428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23328571-T-C

70143434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23328565-C-G

http://identifiers.org/hco/9/GRCh38#70143475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23328482-C-A

70143522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23328375-T-A

70143559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23328221-T-C

70143646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23328134-T-C

70143661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23328119-T-C

70143697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23328083-C-G

http://identifiers.org/hco/9/GRCh38#70143948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23327843-C-A

70144138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327689-T-C

70144150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327677-C-G

70144150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327677-C-T

70144163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327664-T-C

70144165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327662-C-T

70144167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327660-T-A

70144169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327658-T-C

70144267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327565-C-T

http://identifiers.org/hco/9/GRCh38#70144343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23327489-A-C

70144431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327400-G-T

70144557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327276-G-C

70145383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327040-T-C

70145399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327025-T-C

70145401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23327023-G-C

70145440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326996-G-A

70145535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326901-C-G

70145539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326897-T-A

70145539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326897-T-G

70145551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326885-T-C

70145559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326877-C-T

70145685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326787-A-T

70145691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326781-G-A

70145818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326658-T-C

70145885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326594-A-T

70145910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326564-T-C

70146072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326423-T-G

70146332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326160-C-G

70146332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326160-C-T

70146499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326041-G-T

70146500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326040-C-T

70146516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23326025-A-T

70146558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23325980-A-T

70146577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23325949-T-A

70149908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23325131-G-A

70149929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23325110-G-C

70149931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23325108-G-A

70149985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23325058-C-T

70150023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23325030-T-C

70150090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23324990-A-G

70150090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23324990-A-T

70150119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23324977-T-C

70150195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23324905-T-C

http://identifiers.org/hco/9/GRCh38#70150254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23324846-C-A

70150323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23324777-T-C

70150679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23324405-T-C

70151036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23324077-C-T

http://identifiers.org/hco/9/GRCh38#70151094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23324031-A-C

70151337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23323785-T-C

70152497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23323472-C-T

70152549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23323416-A-G

70152716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23323244-C-T

70153004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23322900-T-A

70153004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23322900-T-C

http://identifiers.org/hco/9/GRCh38#70153444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23321711-C-A

70153514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23321652-C-T

70153523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23321643-G-T

70153544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23321615-G-A

70153648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23321512-G-A

70153721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23320559-T-A

http://identifiers.org/hco/9/GRCh38#70153742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23320538-C-A

70153742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23320538-C-G

70153992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23320337-T-C

http://identifiers.org/hco/9/GRCh38#70153993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23320336-C-A

70154139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23320194-T-G

70154181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23320145-A-G

70154181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23320145-A-T

70154256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23320082-G-A

70154290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23320065-C-G

70161208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23317149-G-A

70161280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23317078-C-T

http://identifiers.org/hco/9/GRCh38#70161369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23317030-C-A

70161369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23317030-C-T

70161614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23316780-A-G

70161927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23316447-C-T

70162789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23315930-G-A

70162807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23315915-T-A

70162902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23315842-C-T

70163076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23315698-C-T

70163109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23315665-T-C

70164234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23315073-T-C

70165069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23314715-C-T

http://identifiers.org/hco/9/GRCh38#70165081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23314703-A-C

70165097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23314685-T-C

http://identifiers.org/hco/9/GRCh38#70165364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23314027-A-C

70165477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23313914-C-T

70165497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23313894-T-C

70166358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23313337-C-T

70166385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23313310-T-C

70166385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23313310-T-G

70166418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23313279-C-T

70166579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23313123-A-G

70166635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23313071-A-G

70166657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23313040-A-G

70166787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23312911-G-T

70166798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23312900-A-G

70167127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23312570-G-A

70167219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23312480-T-A

70167219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23312480-T-C

70167507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23312191-T-C

70167875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311950-T-C

70168563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311582-G-A

70168563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311582-G-T

70168570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311575-T-C

http://identifiers.org/hco/9/GRCh38#70168607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23311539-C-A

70168607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311539-C-G

70168607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311539-C-T

70168611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311535-G-A

70168611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23311535-G-T

70168623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23311523-T-C

70168623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23311523-T-G

http://identifiers.org/hco/9/GRCh38#70169141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23310989-C-A

70169203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23310928-T-A

http://identifiers.org/hco/9/GRCh38#70169558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23309345-A-C

70169558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23309345-A-G

70169558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23309345-A-T

70169688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23309236-A-G

70169793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23309124-A-G

70169803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23309112-G-T

70169851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23309002-A-G

70169859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308989-T-G

70170005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308840-A-G

70170043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308836-C-T

70170166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308705-T-A

70170262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308616-T-C

70170263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308615-A-G

70170281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308602-T-C

http://identifiers.org/hco/9/GRCh38#70170312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23308579-C-A

http://identifiers.org/hco/9/GRCh38#70170335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23308560-C-A

70170335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308560-C-T

70170344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308551-G-A

70170344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308551-G-C

70170344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308551-G-T

70170380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308509-A-G

70170458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308421-A-G

70170529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308350-A-G

70170701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308183-G-A

70170701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308183-G-T

70170788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308100-T-C

70170818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308078-T-C

70170818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308078-T-G

70170820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308076-G-T

70170897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23308031-G-A

70170973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23307961-T-C

70172054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23307132-T-G

70172184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23306999-A-G

70172343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23306842-G-C

70172469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23306719-T-C

70172619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23306583-T-A

70172619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23306583-T-C

70172619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23306583-T-G

70172783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23306424-A-G

70172810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23306398-C-T

70173203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23306068-A-T

70173204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23306067-T-C

70173211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23306060-T-C

70173628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23305328-G-T

70173723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23305231-A-G

70175789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 23304972-C-T

70175882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23304889-C-T

http://identifiers.org/hco/9/GRCh38#70175930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23304847-C-A

70176084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23304681-T-A

70176084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23304681-T-C

70176349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23304425-C-T

http://identifiers.org/hco/9/GRCh38#70176399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23304378-A-C

http://identifiers.org/hco/9/GRCh38#70176623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23304214-A-C

70176662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23304175-C-T

70177836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23303751-A-G

http://identifiers.org/hco/9/GRCh38#70178061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23303638-A-C

70192631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23297074-A-G

70192743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23296969-G-A

70192838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23296897-C-G

70192999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23296743-A-T

70193246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23296296-T-C

70193255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23296287-C-T

70193567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23295779-T-C

http://identifiers.org/hco/9/GRCh38#70193690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23295674-A-C

70193753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23295614-G-A

70193826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23295543-T-C

http://identifiers.org/hco/9/GRCh38#70193880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23295488-C-A

70193880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23295488-C-T

http://identifiers.org/hco/9/GRCh38#70193916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23295452-C-A

http://identifiers.org/hco/9/GRCh38#70194059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23295310-C-A

70194169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23295185-C-T

70194192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23295162-G-A

70194192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23295162-G-T

70194654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23295077-G-A

70194654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23295077-G-T

70194911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23294845-C-T

70195245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23294509-A-T

70195362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23294400-A-G

70195381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23294382-C-T

70198468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23294197-G-A

http://identifiers.org/hco/9/GRCh38#70198563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23294117-C-A

70198906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23293644-T-C

70212794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23291666-G-T

70212843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23291617-G-T

70212865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23291596-T-G

70212913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23291550-G-C

70212923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23291535-G-A

70213115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23291351-G-A

70213115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23291351-G-C

70213115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23291351-G-T

http://identifiers.org/hco/9/GRCh38#70213186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23291316-A-C

70213507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23290889-T-C

70213697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23290642-T-C

70213729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23290619-G-T

70213848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23290303-T-A

70213897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23290253-C-T

70214001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23290148-T-C

70214281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23289867-C-T

70218023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23288687-A-G

70218199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23288518-A-G

70218254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23288463-T-C

70218267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23288458-G-A

http://identifiers.org/hco/9/GRCh38#70218271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23288454-A-C

70218271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23288454-A-G

http://identifiers.org/hco/9/GRCh38#70218623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23288098-C-A

70218623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23288098-C-T

70218634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23288087-G-A

70218701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23288021-T-A

70218701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23288021-T-C

70218873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23287830-T-C

70218957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23287775-T-G

70219007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23287728-A-G

70219025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23287710-T-C

70219229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23287541-G-A

70219345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23287449-G-C

70219496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23287295-C-T

70219579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23287208-G-A

70220395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23285972-C-T

70220686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23285704-G-T

70220779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23285609-A-G

70220794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23285594-T-C

70220812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23285576-C-T

70220832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23285554-T-C

70221050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23285317-C-T

70221091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23285277-C-T

70221174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23285192-T-C

70221190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23285174-G-A

70221485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23284826-G-C

70221485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23284826-G-T

70221570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23284751-G-A

http://identifiers.org/hco/9/GRCh38#70221737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23284593-A-C

70221737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23284593-A-G

70221768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23284563-T-C

70221815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23284493-A-G

70221822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23284486-G-A

70221826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23284482-A-T

70221924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23284247-A-G

70221932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23284239-G-A

70221954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23284217-A-G

http://identifiers.org/hco/9/GRCh38#70222008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23284166-A-C

70222027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23284147-G-A

70223383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23283566-T-C

70223389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23283560-T-C

70223424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23283509-T-C

70223456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23283473-T-C

http://identifiers.org/hco/9/GRCh38#70223507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23283423-A-C

70223580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23283352-G-A

70223842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23283119-T-C

70223984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23282968-T-C

70224149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23282812-C-T

70224643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23282443-A-G

70224698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23282388-A-G

70224749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23282338-G-C

70225138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23281969-C-G

70225606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23281401-T-A

70225614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23281393-T-C

http://identifiers.org/hco/9/GRCh38#70225644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23281363-C-A

70225644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23281363-C-T

70225657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23281350-T-G

http://identifiers.org/hco/9/GRCh38#70225679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23281328-C-A

http://identifiers.org/hco/9/GRCh38#70225707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23281299-C-A

70225777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23281231-T-G

70225825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23281183-C-T

70225873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23281136-T-C

http://identifiers.org/hco/9/GRCh38#70225882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23281126-C-A

70225882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23281126-C-T

70225967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23281049-G-A

70225967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23281049-G-T

70226050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23280966-A-G

http://identifiers.org/hco/9/GRCh38#70226066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#23280950-C-A

70226278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23280721-G-T

70226449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23280554-A-G

70226469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23280536-A-T

70226640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23280443-A-G

70226712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23280372-T-C

70226741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23280345-G-A

70226962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23673
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23280115-T-C