http://identifiers.org/hco/5/GRCh38#169013285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35276708-C-A

http://identifiers.org/hco/5/GRCh38#169013295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35276697-C-A

169013295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35276697-C-G

169013295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35276697-C-T

169013313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35276679-T-C

169013314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35276678-C-T

http://identifiers.org/hco/5/GRCh38#169013315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35276677-C-A

169013352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35276667-T-C

169013355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35276664-T-C

169013372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35276648-A-G

http://identifiers.org/hco/5/GRCh38#169013493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35276510-C-A

169013508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35276493-T-C

169013755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35276258-C-G

169013779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35276234-C-T

169013901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35276118-G-C

169014289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35275684-T-C

169014302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35275670-A-G

169014354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35275610-G-A

169014431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35275534-G-T

169014671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35275268-G-A

169014898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35275182-C-T

169015141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35275101-T-C

169015356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35274911-G-A

http://identifiers.org/hco/5/GRCh38#169016055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35274529-C-A

169016400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35274092-C-T

169016509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35273977-T-C

http://identifiers.org/hco/5/GRCh38#169016575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35273907-A-C

169016575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35273907-A-G

169016575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35273907-A-T

http://identifiers.org/hco/5/GRCh38#169016638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35273852-C-A

169016663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35273829-C-G

169016776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35273727-G-A

169016780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35273723-T-G

169017400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35273386-A-G

169017508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35273286-T-G

169017572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35273223-G-A

169017651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35273137-T-C

http://identifiers.org/hco/5/GRCh38#169017671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35273117-A-C

169017671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35273117-A-G

169017722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35273053-T-C

169017781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272982-G-C

169017787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272968-G-T

169017802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272949-G-A

169017802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272949-G-C

http://identifiers.org/hco/5/GRCh38#169017803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35272948-C-A

169017813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272941-G-A

169017842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35272937-G-C

169017874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35272910-G-T

169017905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35272880-G-T

169017970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272804-A-T

169018063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272726-A-G

169018170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272632-A-G

169018170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272632-A-T

169018186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272624-G-A

http://identifiers.org/hco/5/GRCh38#169018215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35272595-C-A

169018268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272546-T-A

169018277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272537-G-A

169018277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272537-G-T

169018278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272536-G-C

169018278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272536-G-T

169018282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272532-G-A

169018282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272532-G-T

169018296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272518-G-A

169018296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272518-G-C

169018353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272462-A-G

169018436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35272386-G-T

169018450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35272372-G-A

169018450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35272372-G-T

169018466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35272349-T-C

169018508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35272307-G-A

169018600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35272221-A-G

169018677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35272132-G-T

169018706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272104-G-T

169018720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272089-A-G

169018721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35272088-A-G

http://identifiers.org/hco/5/GRCh38#169018768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35272042-C-A

169018946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35271879-C-T

169019135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35271676-T-C

169019409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35271242-T-C

169019412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35271239-A-G

169019465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35271164-T-C

http://identifiers.org/hco/5/GRCh38#169019583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35271087-C-A

169019752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35270932-C-T

http://identifiers.org/hco/5/GRCh38#169019872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35270803-A-C

169019921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35270755-C-T

http://identifiers.org/hco/5/GRCh38#169019988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35270692-A-C

169020108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35270589-G-T

169020219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35270471-C-T

169020303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35270391-G-T

169020331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35270363-G-A

169020656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35269995-G-A

169020677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35269983-A-G

169020755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35269899-A-G

169020896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35269783-C-G

169021034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35269640-T-C

169021939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35269164-T-C

http://identifiers.org/hco/5/GRCh38#169022026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35269096-C-A

169022047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35269075-G-T

http://identifiers.org/hco/5/GRCh38#169022059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35269063-C-A

169022105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35268883-G-T

169022126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35268860-A-G

http://identifiers.org/hco/5/GRCh38#169022189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35268791-A-C

169022189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35268791-A-G

169022261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35268720-G-C

169022268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35268713-A-G

169022279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35268702-A-G

169022320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35268662-G-T

http://identifiers.org/hco/5/GRCh38#169022383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35266830-A-C

169022559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35266650-A-G

169022626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35266581-A-G

169022800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35266455-T-C

http://identifiers.org/hco/5/GRCh38#169022803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35266452-C-A

169022803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35266452-C-T

169022814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35266440-A-G

http://identifiers.org/hco/5/GRCh38#169024128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35266274-C-A

169024128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35266274-C-T

169024161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35266236-T-C

169024178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35266219-A-G

169024179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35266218-G-A

http://identifiers.org/hco/5/GRCh38#169024188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35266211-C-A

169024188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35266211-C-T

http://identifiers.org/hco/5/GRCh38#169024193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35266206-C-A

169024280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35266114-G-T

169024472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35265948-A-G

169024486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35265933-T-C

169024627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35265819-G-T

169024678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35265768-G-C

169024734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35265718-T-G

169024795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35265660-A-G

http://identifiers.org/hco/5/GRCh38#169024888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35265557-C-A

169024917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35265530-A-G

169024933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35265514-T-C

169024987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35265459-G-T

http://identifiers.org/hco/5/GRCh38#169025286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35265123-A-C

169025328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35265098-A-G

169025571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35264882-G-A

169025571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35264882-G-T

169025676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35264772-G-A

169025676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35264772-G-C

169025787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35264661-G-A

169025861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35264584-T-C

http://identifiers.org/hco/5/GRCh38#169025968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35264480-A-C

169025976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35264472-A-T

169025984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35264464-A-G

169026001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35264448-C-T

169026351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35263985-T-G

169026473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35263884-A-G

169026484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35263873-T-C

http://identifiers.org/hco/5/GRCh38#169026485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35263872-C-A

http://identifiers.org/hco/5/GRCh38#169026492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35263865-C-A

169026658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35263729-G-T

169026684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35263703-A-G

169026963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35262940-T-C

169026963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35262940-T-G

169027092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35262812-T-G

169027137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35262253-A-G

169027305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35262085-T-C

169027446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35261958-G-A

169027545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35261838-C-T

http://identifiers.org/hco/5/GRCh38#169027656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35261741-C-A

169027656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35261741-C-T

169027688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35261709-C-T

169027716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35261685-G-A

169027716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35261685-G-T

169027898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35261504-T-C

169027932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35261470-A-G

http://identifiers.org/hco/5/GRCh38#169028042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35261369-C-A

169028042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35261369-C-T

169028060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35261351-G-A

http://identifiers.org/hco/5/GRCh38#169028089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35261322-C-A

169028394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35261028-T-C

169028401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35261020-C-T

http://identifiers.org/hco/5/GRCh38#169028664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35260780-A-C

169029869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35259537-T-C

169030195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35259220-C-T

169030359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35259068-C-T

169030372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35259055-T-A

http://identifiers.org/hco/5/GRCh38#169030484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35258938-C-A

169030484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35258938-C-T

http://identifiers.org/hco/5/GRCh38#169030497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35258925-C-A

169030823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35258605-G-T

169030946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35258493-A-G

169030963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35258480-G-C

169030984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35258459-G-A

169031089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35258356-G-A

http://identifiers.org/hco/5/GRCh38#169031201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35258091-C-A

169031238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35258051-T-C

169031244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35258045-T-C

169031331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35257958-G-A

169031331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35257958-G-T

http://identifiers.org/hco/5/GRCh38#169031417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35257903-A-C

169031417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35257903-A-G

http://identifiers.org/hco/5/GRCh38#169031606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35257694-A-C

169032021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35257313-C-T

http://identifiers.org/hco/5/GRCh38#169032117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35257219-C-A

169032119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35257217-A-T

169032128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35257208-G-A

http://identifiers.org/hco/5/GRCh38#169032155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35257181-A-C

169032258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35257077-A-G

169036180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35256866-G-A

169036180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35256866-G-T

169036268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35256787-A-G

169036362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35256703-G-T

169036472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35256593-A-G

169036672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35256390-G-A

169036933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35256135-A-G

169037139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35255951-T-C

169037176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35255921-C-T

169037486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35255595-C-T

169037654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35255428-T-A

169037654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35255428-T-C

http://identifiers.org/hco/5/GRCh38#169037672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35255409-C-A

169037706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35255374-C-T

169037776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35255307-A-G

169037833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35255234-T-C

169037868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35255211-T-G

169037906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35255173-G-A

169037906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35255173-G-T

http://identifiers.org/hco/5/GRCh38#169037943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35255136-C-A

http://identifiers.org/hco/5/GRCh38#169037958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35255122-C-A

http://identifiers.org/hco/5/GRCh38#169037997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#35255089-C-A

169037997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40553
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35255089-C-T