http://identifiers.org/hco/3/GRCh38#71944214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99868631-A-C

71944283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99868700-C-G

71944351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99868748-T-C

71944770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869106-G-T

71944900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869235-C-T

71944904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869239-G-A

71944906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869241-C-T

71945147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869465-T-A

71945147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869465-T-C

71945147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869465-T-G

71945257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99869557-C-T

71949597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99871721-A-G

71949597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99871721-A-T

71949656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99871769-A-T

71949674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99871787-G-A

71949674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99871787-G-T

71950259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99872300-A-G

71950638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99874145-T-C

71950650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99874157-A-T

71950842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99874342-G-C

71950851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99874385-G-C

71951063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99874613-A-G

71951241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99874774-A-G

71951269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99874820-C-T

71951500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875078-A-G

71951538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875112-G-T

http://identifiers.org/hco/3/GRCh38#71951569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99875144-C-A

71951710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99875251-G-T

71952370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99877191-G-A

http://identifiers.org/hco/3/GRCh38#71952411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99877232-C-A

71952411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99877232-C-T

71952471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99877287-C-T

71952526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99877331-G-A

71952682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99877478-G-A

71952758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99877552-C-G

71952820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99877615-G-T

71952903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99877698-G-A

71954630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99880218-T-C

71954929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99880443-A-G

71954966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99880472-T-C

71955034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99880551-C-T

71955314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99880804-C-T

71955439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99880910-A-G

71955490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99880988-A-G

71955819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99881505-G-T

71955922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99881602-A-G

71956416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99882045-G-T

http://identifiers.org/hco/3/GRCh38#71956571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99882169-A-C

71956571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99882169-A-G

71956628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99882225-G-C

71956666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99882262-G-A

71963240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99885137-C-T

71963371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99885246-A-T

71963523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99885375-T-C

71963537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99885388-C-T

71963604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99885464-T-A

71964144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99886460-C-T

71964161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99886477-A-T

71964207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99886498-G-A

71964513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99886812-G-A

71964652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99886929-G-A

71964837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99887120-C-T

71964838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99887121-C-T

71964937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99887223-T-C

71964942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99887228-C-T

71964989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99887278-G-A

71965037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99887325-G-A

71965037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99887325-G-T

71965199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99887445-C-G

71965199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99887445-C-T

71965207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99887453-T-G

71965257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99887485-T-C

71965898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99887764-A-G

71965987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99887836-C-T

71966255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99888084-T-A

http://identifiers.org/hco/3/GRCh38#71966291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99888116-C-A

71966292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99888117-C-T

71966293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99888118-G-A

71966303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99888128-G-A

71966659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99888431-C-T

71966863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99888619-C-T

71966915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99888668-A-T

71967121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99889053-T-C

71967257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99889217-T-C

71967748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99889647-G-T

71967769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99889667-C-T

71969002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99890502-G-A

71969057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99890554-C-T

71971738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99890897-A-G

71971860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99891003-G-A

71971910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99891054-A-G

71972054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99891193-T-G

71972146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99891253-G-T

71972443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99891552-G-T

71972497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99891598-T-C

71974523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893401-G-A

71974670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893545-T-C

71974673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893548-T-C

71974673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893548-T-G

71974901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893774-A-T

71974957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893828-G-A

71975087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99893977-C-T

71975127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99894022-G-A

71975357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99894265-C-T

71975522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99894352-G-T

71975575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99894404-C-T

71975754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99895236-C-T

71975830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99895303-G-A

71975846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99895319-A-G

71976015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99895494-C-T

71976057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99895536-G-C

71976307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99895764-G-A

71976371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99895828-C-T

71977721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99896567-G-A

71977813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99896650-A-G

71977856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99896691-A-G

http://identifiers.org/hco/3/GRCh38#71983719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99897111-C-A

71983719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99897111-C-T

71984017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99897357-C-T

71984106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99897444-C-T

71984161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99897499-T-C

71984184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99897522-T-C

71986440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99900073-C-T

71986472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99900113-G-A

71986503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99900142-G-A

71986503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99900142-G-C

71986503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99900142-G-T

71986756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99900361-T-G

71986863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99900463-T-G

71986882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99900476-A-G

71987835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99901183-C-T

71987860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99901208-C-T

71988349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99901671-A-G

71988349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99901671-A-T

71988400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99901728-T-A

http://identifiers.org/hco/3/GRCh38#71988554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99901883-A-C

71988554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99901883-A-G

71989022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902034-G-C

71989033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902045-T-C

71989071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902100-A-G

71989071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902100-A-T

71989372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902370-T-C

71989452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902410-A-T

71989586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902538-A-G

71989590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902542-G-T

71989929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902646-T-C

71990026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902737-G-A

71990083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902778-C-T

71990228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902895-T-C

71990309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902976-T-C

71990311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99902978-C-T

http://identifiers.org/hco/3/GRCh38#71991922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99905005-A-C

71991985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99905048-G-A

71991989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99905052-G-A

71991990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99905053-T-C

71991994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99905057-T-C

71992102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99905165-A-G

71992260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99905251-G-A

71992260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99905251-G-C

71992394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99905372-G-A

71995713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99905843-T-G

71995760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99905885-T-C

71995808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99905946-G-A

71995898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99906052-G-T

71996307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99906443-T-A

71996307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99906443-T-C

71996928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99907197-T-G

71997192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99907438-C-G

72008442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99907980-C-T

72008531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908069-T-A

http://identifiers.org/hco/3/GRCh38#72008558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99908088-C-A

72008562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908092-T-C

72008633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908148-G-T

72008643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908157-G-C

72008749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908226-T-C

72008829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908294-G-A

72008924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908350-T-C

72008981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908406-G-A

72009014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908442-T-A

http://identifiers.org/hco/3/GRCh38#72009483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99908869-C-A

72009521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99908892-C-T

http://identifiers.org/hco/3/GRCh38#72010271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#99909587-A-C

72011078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99911171-C-G

72011463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99911486-C-T

72011865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99911877-A-G

72011865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99911877-A-T

72012349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99912738-A-G

72012349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99912738-A-T

72012408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99913378-G-A

72012420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99913390-T-C

72012664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99913637-T-A

72012664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99913637-T-C

72012678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99913651-G-A

72012804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99913805-T-C

72014060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99914210-G-A

http://identifiers.org/hco/3/GRCh38#72014183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99914389-A-C

72014295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99914521-C-T

72014762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99915285-C-G

72014900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99915407-A-G

72015096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99915604-C-T

72015154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99915659-C-T

72015399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99915926-C-T

72017323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99916112-T-A

72017323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99916112-T-C

72017391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99916171-T-A

http://identifiers.org/hco/3/GRCh38#72017608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99916395-A-C

http://identifiers.org/hco/3/GRCh38#72017633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99916420-C-A

72017633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99916420-C-G

http://identifiers.org/hco/3/GRCh38#72017703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99916466-A-C

72017736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99916499-T-C

72017736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99916499-T-G

72018236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99917021-C-T

72018381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99917157-C-T

72018823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99917489-T-C

72018863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99917520-A-G

72030906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99921169-G-T

72031005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99921265-G-A

72031114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99921389-G-A

http://identifiers.org/hco/3/GRCh38#72032847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99923630-C-A

72032912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99923682-C-T

72033136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99923896-T-C

72033529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99924212-G-C

http://identifiers.org/hco/3/GRCh38#72033560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99924246-C-A

72033606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99924290-C-G

72033692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99924339-G-A

72033803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99924423-G-A

72034394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99924736-T-C

http://identifiers.org/hco/3/GRCh38#72034516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99924861-C-A

72034677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99924993-T-C

http://identifiers.org/hco/3/GRCh38#72034697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99925011-C-A

72034698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99925012-C-T

http://identifiers.org/hco/3/GRCh38#72034875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99925154-A-C

72035248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99925625-A-G

72035262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99925639-G-A

72035262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99925639-G-T

72035305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99925682-A-G

72035307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99925687-G-A

72035307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99925687-G-T

72035335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99925705-G-A

72035335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99925705-G-T

http://identifiers.org/hco/3/GRCh38#72039365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99927397-A-C

72039423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99927460-G-C

72040818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99931175-C-T

72040886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99931231-C-T

72040957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99931278-T-C

72041195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99931493-C-T

72041538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99931833-G-C

72041622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99931927-A-G

72041637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99931942-G-A

72041642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99931947-G-C

http://identifiers.org/hco/3/GRCh38#72041715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99932024-A-C

72041869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932178-G-A

72041888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932197-G-A

72042140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932391-T-C

72042259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932495-G-C

72042372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932609-A-G

72042390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932614-C-T

72042399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932623-A-G

72042498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932708-G-A

72042608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932799-T-C

72042670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99932843-G-C

72042870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99933078-G-A

72042925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99933134-G-A

72043720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99935604-G-T

72044178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936011-C-G

72044409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936307-A-G

72044417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936315-T-A

72044577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936455-C-T

72044655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936536-G-A

72046223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936636-C-T

72046471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936867-C-G

72046471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99936867-C-T

72048167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99937768-T-C

72048190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99937791-G-A

72048194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99937795-C-G

72048203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99937804-C-T

72048226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99937827-A-G

72048405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99937980-C-T

72048427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938002-G-T

72048568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938106-G-A

72048628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938159-C-T

72048719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938260-T-C

72048768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938297-T-C

http://identifiers.org/hco/3/GRCh38#72048857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99938385-A-C

72048860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938388-C-T

72048899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99938427-C-T

http://identifiers.org/hco/3/GRCh38#72049069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99938777-C-A

72049542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940611-C-T

72049650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940709-A-T

72049661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99940718-G-A

72050204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99941496-G-T

72050278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99941572-T-C

72050382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99941674-C-G

72051302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99944058-A-G

72051370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99944113-C-T

72051425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99944164-T-C

72051760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99944516-C-T

72051976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99944726-A-G

http://identifiers.org/hco/3/GRCh38#72052011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99944761-C-A

72052232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99944941-G-T

72052331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99945009-G-A

72052331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99945009-G-C

72055280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99945714-G-A

72055460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99945884-A-G

72055543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99945986-T-C

72055555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99945997-C-G

72056049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99946483-C-T

72056125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99946550-G-C

http://identifiers.org/hco/3/GRCh38#72056162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99946580-A-C

72058366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99948256-T-C

http://identifiers.org/hco/3/GRCh38#72058398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99948292-A-C

http://identifiers.org/hco/3/GRCh38#72058647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99948525-C-A

72060823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99949189-A-G

http://identifiers.org/hco/3/GRCh38#72060855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99949237-C-A

72060855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99949237-C-T

72060863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99949250-T-C

72060865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99949252-G-T

72060871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99949257-T-C

72060907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99949303-G-T

72060928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99949323-C-T

http://identifiers.org/hco/3/GRCh38#72060958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99949342-A-C

http://identifiers.org/hco/3/GRCh38#72061038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99949422-C-A

http://identifiers.org/hco/3/GRCh38#72061047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99949431-C-A

72061047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99949431-C-T

72061056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99949439-G-T

72061083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99949454-C-T

http://identifiers.org/hco/3/GRCh38#72061084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99949455-C-A

72061103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99949465-G-A

72061141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99949503-G-A

72061183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99949541-C-T

72061261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99949629-T-C

72061642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951068-T-C

72061827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951245-G-T

72061939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99951354-G-A

72062019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951433-G-T

http://identifiers.org/hco/3/GRCh38#72062311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99951713-C-A

72062311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951713-C-G

72062311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951713-C-T

http://identifiers.org/hco/3/GRCh38#72062562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99951926-C-A

http://identifiers.org/hco/3/GRCh38#72062570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99951934-C-A

72062592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99951956-A-G

72071809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99955561-C-T

72071983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99955696-G-A

72072055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99955773-T-C

72072217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99955897-T-A

72072217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99955897-T-C

72072364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99956038-G-A

72072404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99956078-T-C

http://identifiers.org/hco/3/GRCh38#72072537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99956210-A-C

http://identifiers.org/hco/3/GRCh38#72072905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99956805-A-C

72075236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99958887-G-A

72075270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99958923-G-A

72075286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99958945-G-T

72075320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99958979-G-A

72075320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99958979-G-T

72075349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99959008-A-G

72075478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99959112-G-C

72077669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99961059-T-C

72077738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99961123-T-C

72078158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99961584-G-C

72078260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99961674-T-G

72078320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99961863-A-T

72078344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99961885-C-T

72078356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99961894-T-C

72078701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99962238-C-G

72078721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99962258-G-A

72078788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99962333-T-C

72079039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99962572-C-G

72079213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99962731-C-T

72079400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99962926-C-T

72079450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99962989-A-G

http://identifiers.org/hco/3/GRCh38#72079495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99963034-C-A

72079495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99963034-C-T

72079705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99963407-G-T

72079833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99963714-C-T

72079966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99963867-T-C

72080310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99964160-G-T

72080430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99964234-T-C

72080456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99964258-T-C

72091904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99967802-A-G

72092197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99968043-C-T

72092349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99968218-A-G

72092434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99968284-T-A

72092459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99968309-G-T

72094534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99970162-G-A

72094584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99970204-G-T

72095457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99970862-G-C

72095632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99971022-T-C

72095989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99971346-C-T

72096071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99971386-A-G

72096279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99971543-T-C

72096356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99971620-T-C

72097219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99973346-T-C

72097513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99973610-C-T

http://identifiers.org/hco/3/GRCh38#72097662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99973738-C-A

72097662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99973738-C-G

72097662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99973738-C-T

http://identifiers.org/hco/3/GRCh38#72097675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99973751-C-A

72097675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99973751-C-T

72097720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99973796-G-T

72097815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99973891-G-T

72097916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974060-G-C

72097916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974060-G-T

72097934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974084-G-A

72097934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974084-G-T

http://identifiers.org/hco/3/GRCh38#72098032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99974406-C-A

72098032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974406-C-T

72098076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974453-T-A

72098100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974490-G-A

72098100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974490-G-C

72098100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974490-G-T

72098154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974533-G-T

72098200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974570-G-T

http://identifiers.org/hco/3/GRCh38#72098203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99974573-C-A

72098203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974573-C-T

72098258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974682-A-G

72098303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974714-C-T

http://identifiers.org/hco/3/GRCh38#72098322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99974731-C-A

72098338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974747-G-A

72098338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974747-G-T

72098392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974810-A-G

72098392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974810-A-T

72098402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974820-A-T

http://identifiers.org/hco/3/GRCh38#72098411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99974828-C-A

72098411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974828-C-T

72098423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974840-C-T

72098446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974857-T-C

72098530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974893-G-A

72098551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974914-T-C

72098593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974950-T-C

72098621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974975-T-A

72098621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99974975-T-G

72098683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99975019-C-T

72098853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99975101-G-A

72098853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99975101-G-C

72098853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99975101-G-T

72098900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99975142-G-A

72098900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99975142-G-T

72098977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99975186-C-G

72098977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99975186-C-T

http://identifiers.org/hco/3/GRCh38#72098984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99975193-C-A

72099005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99975214-G-A

72099005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99975214-G-T

72099026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99975225-A-G

72099139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99975330-G-T

72099249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99975425-C-T

72099281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99975458-G-A

72099838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99976021-A-G

http://identifiers.org/hco/3/GRCh38#72099841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99976024-C-A

72099917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: non coding transcript exon variant
orthologous variants: 99976089-G-A

72099917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: non coding transcript exon variant
orthologous variants: 99976089-G-C

72099985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: non coding transcript exon variant
orthologous variants: 99976157-G-A

72099985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: non coding transcript exon variant
orthologous variants: 99976157-G-T

http://identifiers.org/hco/3/GRCh38#72100005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99976177-A-C

72100005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 99976177-A-G

72100166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99976334-C-G

http://identifiers.org/hco/3/GRCh38#72100291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99976453-C-A

72100320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99976486-A-G

72100320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99976486-A-T

72100349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99976506-T-C

http://identifiers.org/hco/3/GRCh38#72100641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#99976817-C-A

72100641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99976817-C-G

72100641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99976817-C-T

http://identifiers.org/hco/3/GRCh38#72100676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#99976852-C-A

72100676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99976852-C-T

72100685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99976861-C-T

72100714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99976901-G-A

72100714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99976901-G-C

72100714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99976901-G-T

72100803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99976987-G-A

http://identifiers.org/hco/3/GRCh38#72100938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99977095-C-A

72100938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99977095-C-T

http://identifiers.org/hco/3/GRCh38#72100970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99977107-C-A

72100970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99977107-C-T

72100972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99977109-G-T

http://identifiers.org/hco/3/GRCh38#72101006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#99977141-C-A

72101006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99977141-C-G

72101006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99977141-C-T

72101010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99977145-G-A

72101108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99977252-C-T

72101149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99977281-A-G

72101723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99978312-A-G

72101726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99978318-T-C

72102014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99978664-G-A

72102020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99978669-C-T

http://identifiers.org/hco/3/GRCh38#72102118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99978755-C-A

72102146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99978783-G-C

72102269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99978910-T-C

72102284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99978925-G-T

72102560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99979064-C-T

72102709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99979279-G-A

72102759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99979443-C-T

http://identifiers.org/hco/3/GRCh38#72102788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99979472-C-A

72102788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99979472-C-G

72102792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99979476-T-C

72106100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99981975-T-C

72106255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99982131-T-G

72106273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99982154-A-G

72106278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99982159-C-T

72106334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99982209-A-G

72106346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99982221-G-T

72106389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99982647-A-G

72106534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99982790-A-G

72106669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99982921-C-T

72106792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99983039-G-C

72106792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99983039-G-T

72106938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99983198-A-G

72107022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99983279-A-G

72107040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99983304-G-A

72110746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987715-T-A

72110770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987739-G-A

72110949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987898-G-A

72110949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987898-G-T

72110950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99987899-G-A

72112102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99989027-C-T

72112242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99989165-G-A

72112304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99989211-C-T

72112327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99989234-T-C

72112481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99989415-G-A

72112614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99989529-G-A

72112923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99989823-T-A

72112923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99989823-T-C

72113122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99990006-C-T

72113446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99990817-G-A

72113532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99990904-T-C

http://identifiers.org/hco/3/GRCh38#72113864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99991262-C-A

72114036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99991439-T-G

72115221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99993026-G-A

72115916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99994909-G-C

72115938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99994931-G-C

72116373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99995077-G-A

72116498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99995170-A-G

72116499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99995171-T-C

72116504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99995176-C-T

72116653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99995344-C-T

72116657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99995348-G-A

72119881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997568-A-T

72120211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997872-C-T

72120213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99997874-C-T

72120441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99998102-G-A

http://identifiers.org/hco/3/GRCh38#72120514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#99998176-A-C

72121694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999094-A-G

72121818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999186-A-T

72121840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999208-C-T

72122059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999400-G-A

72122204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999512-C-T

72122228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999537-C-G

72122313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99999623-T-G

72122696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100000231-A-G

72123522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100001576-C-T

72123707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100002145-G-A

72123786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100002225-A-G

72124283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100002694-T-A

72124598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100003018-G-A

72124739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100003201-A-T

72125166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100003502-C-T

72125518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100003819-T-C

72125518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100003819-T-G

72125637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100003922-T-G

72125841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100004075-G-A

72125854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100004086-C-G

72127034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100007349-A-G

72127401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100007716-A-G

72127598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008182-G-T

72127599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008183-T-C

72127651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008233-G-A

72127796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008345-C-T

72127829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008378-A-G

72127876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008429-A-G

72128002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008530-C-T

http://identifiers.org/hco/3/GRCh38#72128034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100008555-C-A

http://identifiers.org/hco/3/GRCh38#72128048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100008566-A-C

72128051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008569-G-C

72128187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008683-G-C

72128213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008699-T-C

72128237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008717-G-T

72128279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008759-C-T

72128370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100008838-C-T

72129346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009605-C-T

72129393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009657-T-G

72129432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100009716-G-A

http://identifiers.org/hco/3/GRCh38#72129636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100009907-C-A

72129926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010191-A-G

72132861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010403-G-C

72132973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010508-A-G

72133275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010782-G-A

72133275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010782-G-T

72133304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010823-G-C

72133338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010858-C-G

72133347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010867-A-T

72133364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100010884-T-A

72136055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100012477-T-C

http://identifiers.org/hco/3/GRCh38#72136200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100012644-C-A

http://identifiers.org/hco/3/GRCh38#72136380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100012837-C-A

72136743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013277-C-G

72136743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013277-C-T

72137215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013824-G-A

http://identifiers.org/hco/3/GRCh38#72137227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100013836-C-A

72137227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013836-C-T

72137228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013837-G-A

72137246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013839-C-T

72137514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013949-A-G

72137554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100013998-A-T

72137602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014045-C-T

72137665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014090-A-G

72137945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014353-G-A

http://identifiers.org/hco/3/GRCh38#72138104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100014508-C-A

72138104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014508-C-G

72138226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014622-G-A

72138241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014637-G-C

72138242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014638-C-T

72138559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100014933-G-C

http://identifiers.org/hco/3/GRCh38#72138561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100014935-C-A

72138605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100015003-G-C

http://identifiers.org/hco/3/GRCh38#72138703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100015095-A-C

72138718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100015109-G-A

72138718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100015109-G-T

72138753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100015144-C-T

72144668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100017348-G-A

72144668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100017348-G-T

http://identifiers.org/hco/3/GRCh38#72145020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100017710-C-A

72145485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018130-T-C

72145490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018135-G-C

72145593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018221-G-A

72145675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018270-C-T

72145688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018282-C-T

72145829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018389-G-T

72145838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018398-G-A

72145890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018450-C-T

72145918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018477-T-C

72146201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018730-G-C

72146227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018755-A-G

72146227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018755-A-T

72146237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018765-G-C

72147732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100018937-A-G

72147948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100019141-A-G

72148092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100019288-G-C

72148271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100019423-C-G

72148271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100019423-C-T

72148421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100019519-C-T

http://identifiers.org/hco/3/GRCh38#72149209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100020200-A-C

72149266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100020261-G-A

72149525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100020578-T-C

72149663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100020709-A-G

72149750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100020789-G-A

72149750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100020789-G-T

72149768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100020810-A-G

72149819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100020861-T-C

72149933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100020993-C-T

72150840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021145-C-T

72150841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021146-A-G

72150841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021146-A-T

http://identifiers.org/hco/3/GRCh38#72150843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100021148-C-A

72150964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021383-C-G

72150971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021390-C-G

72150971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021390-C-T

72151047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021446-C-T

http://identifiers.org/hco/3/GRCh38#72151133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100021482-C-A

http://identifiers.org/hco/3/GRCh38#72151215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100021550-C-A

72151271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100021606-G-A

72151278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100021609-G-T

72151316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100021647-C-T

72151375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100021708-T-C

72151398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100021731-A-G

72151410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100021773-G-T

72151539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021922-A-G

72151679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100021999-C-T

72151872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022172-C-T

72152062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022325-C-T

72152227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022473-C-T

72152393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022609-G-A

72152620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022784-T-C

http://identifiers.org/hco/3/GRCh38#72152635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100022799-C-A

72152635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100022799-C-T

72152660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100022823-G-A

72152660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100022823-G-T

72152731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100022856-A-G

72152918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 100023005-G-A

72152918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 100023005-G-C

72152918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 100023005-G-T

72152927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100023018-C-G

72152927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100023018-C-T

72152930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100023021-T-C

http://identifiers.org/hco/3/GRCh38#72152939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100023030-C-A

72152945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100023036-G-A

72152945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100023036-G-C

72152945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100023036-G-T

72152956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100023046-C-T

http://identifiers.org/hco/3/GRCh38#72152974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100023064-C-A

72152982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100023072-G-A

72153024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100023111-T-G

72153068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100023153-A-G

http://identifiers.org/hco/3/GRCh38#72153075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100023160-C-A

http://identifiers.org/hco/3/GRCh38#72153083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100023168-C-A

72153083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100023168-C-T

72153152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100023234-C-G

72153269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100023356-G-A

72153314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100023400-A-G

72153702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100023748-C-T

http://identifiers.org/hco/3/GRCh38#72154153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100024126-C-A

72154222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100024191-T-C

72158834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028124-C-T

72158843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028133-G-A

72159073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028365-C-T

72159173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028461-G-A

72159173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028461-G-C

72159187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028475-C-T

72159200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028485-G-A

72159230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028520-G-T

72159232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028522-G-T

http://identifiers.org/hco/3/GRCh38#72159290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100028575-C-A

72159313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028598-G-A

http://identifiers.org/hco/3/GRCh38#72159333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100028614-C-A

http://identifiers.org/hco/3/GRCh38#72159400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100028671-C-A

72159456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100028722-G-T

72159543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028766-G-A

72159543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028766-G-C

72159543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028766-G-T

72159579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028773-C-T

http://identifiers.org/hco/3/GRCh38#72159596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100028783-C-A

72159628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028809-A-G

http://identifiers.org/hco/3/GRCh38#72159667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100028853-C-A

72160236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030821-T-G

72160304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030880-T-G

72160338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030908-C-T

72160494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031059-G-A

72160505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031070-C-T

72160527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031091-A-G

72160529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031093-T-C

72160529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031093-T-G

72160573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031136-A-T

72160933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031461-G-A

http://identifiers.org/hco/3/GRCh38#72167305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100032636-A-C

72167305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100032636-A-T

72167488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100032807-G-T

72167783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100032965-G-A

72168032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100033119-C-T

http://identifiers.org/hco/3/GRCh38#72168033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100033120-A-C

72168051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100033122-C-T

72168059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100033130-T-G

http://identifiers.org/hco/3/GRCh38#72168135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100033202-C-A

http://identifiers.org/hco/3/GRCh38#72168779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100033301-C-A

72169100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100033619-C-T

72169412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100033908-T-C

72169570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034029-G-T

72169727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034466-G-A

72169889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034589-T-C

72169898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100034598-A-G

72170103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034747-G-A

72170345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034958-G-T

http://identifiers.org/hco/3/GRCh38#72170374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100034974-C-A

72170383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034978-A-G

http://identifiers.org/hco/3/GRCh38#72170502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100035669-A-C

72170547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035716-G-T

72170567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035736-G-C

72170894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035782-G-A

72171011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035899-A-T

72171340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036228-T-C

72171401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036280-G-A

72171401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036280-G-C

72171609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036489-G-C

72171649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036528-C-T

72171777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036640-T-A

72171777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036640-T-C

http://identifiers.org/hco/3/GRCh38#72171784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100036647-A-C

72171784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036647-A-G

http://identifiers.org/hco/3/GRCh38#72171794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100036657-A-C

72171794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036657-A-G

http://identifiers.org/hco/3/GRCh38#72171906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100036768-C-A

72171991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100036848-G-A

72172403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100037250-G-A

72172403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100037250-G-T

72172545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100037377-A-G

72173071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040115-T-G

72173092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040136-T-C

72173152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040196-G-T

72173235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040268-T-C

72173254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040287-C-T

http://identifiers.org/hco/3/GRCh38#72173311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100040320-C-A

72173320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040329-T-C

72173446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040434-A-G

72173455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040443-T-G

http://identifiers.org/hco/3/GRCh38#72173498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100040472-C-A

72173498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040472-C-T

72173501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040475-T-C

http://identifiers.org/hco/3/GRCh38#72173525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100040532-C-A

72173525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040532-C-G

72173531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040538-C-T

72173661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040703-G-A

72173661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040703-G-T

72174201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100041464-T-C

72174300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100041578-G-T

72174453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100041686-A-G

72174508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100041722-C-T

http://identifiers.org/hco/3/GRCh38#72174516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100041730-A-C

72174516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100041730-A-G

http://identifiers.org/hco/3/GRCh38#72174820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100041985-C-A

72175026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100042147-C-T

72175149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100042257-A-G

72175280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100042523-T-C

72175345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100042584-C-T

72175361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100042605-C-T

72175389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100042635-A-G

72175669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043837-C-T

72175768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043923-C-G

72175804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043959-G-A

72175814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043982-C-T

72175819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043987-T-C

72175819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043987-T-G

http://identifiers.org/hco/3/GRCh38#72175846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100044014-C-A

72176879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044151-C-T

72177216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044393-G-A

72177263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044442-G-A

72177303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044474-C-T

72177598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044754-T-C

72177607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100044763-G-T

72178380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046359-G-A

72178380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046359-G-T

72178388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046367-G-A

72178388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046367-G-C

72178388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046367-G-T

72178396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046375-G-A

72178396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046375-G-T

72178478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046458-A-G

72178478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046458-A-T

72178537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046504-G-T

http://identifiers.org/hco/3/GRCh38#72178602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100046578-C-A

72178611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046587-C-T

72178617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046593-G-A

http://identifiers.org/hco/3/GRCh38#72178656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100046639-C-A

72178814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100046778-T-A

72178814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100046778-T-C

72179135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100047184-G-A

72179939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100048070-G-T

72182778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100051526-G-A

72183030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100051733-C-T

72183068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100051767-G-A

72183355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100052034-T-C

72184505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100052374-T-C

72185997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100056073-C-T

72185998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100056074-T-C

72186259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100056348-T-C

72189815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100057819-C-T

72189820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100057824-G-A

72189855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100057860-G-C

72191073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059091-T-C

72191176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059178-T-C

72191193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059195-G-A

72191339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059342-G-C

72191430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059432-G-C

72191439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059441-C-T

72191469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059471-C-T

72191482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059484-G-A

72191507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059508-T-C

72191509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059510-G-A

http://identifiers.org/hco/3/GRCh38#72191521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100059515-C-A

http://identifiers.org/hco/3/GRCh38#72191572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100059563-A-C

72191572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059563-A-G

72191572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059563-A-T

72191575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059566-T-A

72191575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059566-T-C

72191836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059788-A-G

72192022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059981-A-G

72192075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100060033-A-G

72192089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100060047-C-T

72192693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100060609-C-G

72192693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100060609-C-T

72192794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100060685-C-T

72193171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100061865-T-C

72193659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100062488-C-T

72193930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100062781-C-G

72194391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100063190-C-T

72194424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100063223-C-T

72195686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100063727-T-C

72195751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100063795-T-G

72195882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100063893-C-T

72195894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100063905-C-T

72195896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100063907-A-G

72196176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064128-C-T

72196224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064151-G-A

72196224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064151-G-T

72196271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064192-T-C

72196307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064227-T-C

72196564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064484-G-A

72196590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064510-C-G

72196612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064531-G-C

72196612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064531-G-T

72197613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100065924-T-A

72197728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100066034-A-T

72197781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100066078-G-C

72197816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100066112-G-A

72198010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100066242-C-T

72198400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100066741-T-C

http://identifiers.org/hco/3/GRCh38#72198493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100066830-C-A

72198495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100066832-A-G

72202647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100068187-G-T

72202772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100068301-G-A

72203010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100068521-G-T

72203258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100068749-T-C

72203377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100068912-T-A

72203444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100068991-G-T

72203479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069029-A-G

72203517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069067-A-G

72203523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069073-G-T

72203629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069172-G-A

72203767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069288-T-A

72203780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069303-C-T

72203917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069411-A-G

72203966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069460-G-A

72203966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069460-G-T

72204018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069512-G-A

72204043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069539-G-A

72204043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069539-G-T

http://identifiers.org/hco/3/GRCh38#72204063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100069560-A-C

72204063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069560-A-G

72204102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069593-T-C

72204162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100069657-G-A

72204268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069752-T-C

72204318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069803-G-A

72204318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069803-G-T

http://identifiers.org/hco/3/GRCh38#72204789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100070217-A-C

72204885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100070260-T-A

72204885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100070260-T-C

72204892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100070264-A-G

72204976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100070355-G-A

72205034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100070409-G-A

72205589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100072773-T-A

72205602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100072786-G-A

72205625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100072809-G-A

72205625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100072809-G-T

72205638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100072821-C-G

72205651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100072834-G-A

72205930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100073053-C-T

72206247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100073375-G-C

72206255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100073383-G-T

72206518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100073649-A-G

72207255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100074989-G-A

72207363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100075086-G-A

72207503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100075207-G-T

72207649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100075359-C-T

72207767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100075476-G-A

72209726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100076931-T-C

72209737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100076940-T-C

http://identifiers.org/hco/3/GRCh38#72209811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100076994-C-A

72209826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100077011-T-G

72209829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100077014-G-T

72209934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100077113-G-C

72209934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100077113-G-T

72210203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100077374-T-A

72210244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100077416-G-A

72210586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100077759-G-A

72210607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100077780-C-T

http://identifiers.org/hco/3/GRCh38#72210753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100077939-A-C

72210753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100077939-A-T

72210842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100078024-G-A

72210842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100078024-G-C

72210886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100078057-C-T

72220948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100079795-A-G

http://identifiers.org/hco/3/GRCh38#72221023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100079876-C-A

72221063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100079921-G-A

72221063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100079921-G-T

72221524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100080427-T-C

72221771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100080664-C-G

72221858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100080732-C-T

72222015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100080874-A-G

72222070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100080915-C-T

72222905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100081214-C-T

72223012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100081315-T-G

72223187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100081494-T-G

72223264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100081571-A-G

72223351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100081662-C-T

72223481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100081799-T-C

72223552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100081869-C-T

72223843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100082149-T-C

72223968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100082267-C-T

72224114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100082374-T-G

72224390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100082626-T-A

72224390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100082626-T-C

72224489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100082725-T-C

72224514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100082750-C-T

72224757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100082949-A-G

72225407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100083388-C-T

72225825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100083649-T-C

72225912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100083736-T-G

http://identifiers.org/hco/3/GRCh38#72225935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100083752-C-A

72225976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100083782-T-G

72226075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100083880-A-T

72226105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100083922-T-C

72226113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100083930-G-A

72226148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100083989-C-T

72226283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100084090-T-C

72226332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100084139-T-A

72226334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100084141-C-T

72226783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100085139-T-C

72227119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100085477-C-T

72227210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100085557-A-T

72227848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100088094-G-A

72228112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100088389-G-C

http://identifiers.org/hco/3/GRCh38#72228273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100088509-C-A

72228293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100088525-G-A

http://identifiers.org/hco/3/GRCh38#72228360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100088587-C-A

72228372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100088596-C-G

http://identifiers.org/hco/3/GRCh38#72228799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100088949-C-A

72228877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100089025-T-C

72228891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100089039-A-G

72229025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100089701-T-C

72229150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100089782-C-T

72229471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100090007-G-A

72229512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100090045-C-T

72229839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100090581-T-C

http://identifiers.org/hco/3/GRCh38#72230042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100090775-A-C

72230174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100090901-T-C

72230264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100090992-G-A

72230370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100091048-G-A

72230371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100091049-A-G

72230371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100091049-A-T

72230501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100091156-C-T

72231502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100091926-A-G

72231502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100091926-A-T

72231899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100092302-T-A

72231908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100092311-A-G

http://identifiers.org/hco/3/GRCh38#72231938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100092339-C-A

72231944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100092345-C-T

72232091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100092474-C-G

72232388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100092883-T-C

http://identifiers.org/hco/3/GRCh38#72232415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100092910-C-A

72232484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100092979-G-A

72232671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100093116-C-T

72232678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100093121-G-A

72232678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100093121-G-C

72232718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100093166-G-C

72233721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100093320-G-A

72233779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100093367-C-T

72233955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100093531-C-G

72233964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100093540-G-C

72234043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100093599-T-C

72234064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100093601-C-T

http://identifiers.org/hco/3/GRCh38#72234073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100093610-C-A

72234074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100093611-T-C

http://identifiers.org/hco/3/GRCh38#72234136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100093652-C-A

72234231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100093735-A-G

72234242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100093757-T-C

72234289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100093846-A-T

72234352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100093899-G-C

72234378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100093924-C-T

72234555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100094124-G-A

http://identifiers.org/hco/3/GRCh38#72234582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100094154-A-C

72234646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100094205-A-G

72234696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100094259-G-A

72235014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100094556-G-C

72235195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100094658-C-T

72235225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100094688-G-A

72235225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100094688-G-T

http://identifiers.org/hco/3/GRCh38#72235240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100094705-A-C

72235299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100094771-A-T

72235338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100094809-C-T

72235365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100094831-C-G

72235451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100094922-T-C

72235451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100094922-T-G

72235482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100094951-C-T

http://identifiers.org/hco/3/GRCh38#72237778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100096893-C-A

72238229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100097302-T-G

72238268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100097321-C-G

72238386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100097398-G-A

72238543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100097542-C-T

72240008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100100673-G-C

72240103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100100763-A-G

72240167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100100831-T-C

72240324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100100962-G-A

http://identifiers.org/hco/3/GRCh38#72240422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100101057-C-A

72240422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100101057-C-T

72240477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100101111-C-T

72240514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100101148-T-G

72240775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100101365-C-T

72241123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100101661-A-G

72241272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100101757-G-C

72241357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100101837-C-T

72241441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100101893-G-A

72241544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100101979-T-C

72243503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100102970-C-T

72243696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100103160-G-C

72244007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100103427-T-A

72244343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100103728-C-G

72244365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100103749-G-A

72244365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100103749-G-T

72244375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100103759-G-C

72244437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100103820-G-A

72244566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100103955-T-A

http://identifiers.org/hco/3/GRCh38#72244671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100104049-C-A

72244681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100104054-G-A

72244681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100104054-G-C

72244684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100104057-G-T

72244695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100104068-G-A

72244695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100104068-G-T

72245057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100104370-C-T

http://identifiers.org/hco/3/GRCh38#72245069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100104374-C-A

72245107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100104411-G-C

http://identifiers.org/hco/3/GRCh38#72245366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100104667-A-C

http://identifiers.org/hco/3/GRCh38#72246026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100105287-C-A

72246599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100106175-T-C

72246599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100106175-T-G

http://identifiers.org/hco/3/GRCh38#72247234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100106673-C-A

72247291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100106709-C-T

72247292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100106710-G-A

72247292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100106710-G-T

72247356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100106813-G-A

72247586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100107146-G-A

72247615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100107177-T-C

72247676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100107260-C-T

72247835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100107399-C-T

72247836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100107400-T-G

72248106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100107612-T-C

http://identifiers.org/hco/3/GRCh38#72248341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100107803-A-C

72251057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100109902-A-G

72251090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100109935-G-A

72251091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100109936-C-T

72251120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100109966-G-T

72251290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100110123-C-G

72251290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100110123-C-T

72251416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100110233-C-T

72251548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100110322-C-T

72251821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100110487-A-G

72251863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100110519-T-C

72255154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100115394-G-A

72255225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100116866-T-A

http://identifiers.org/hco/3/GRCh38#72255538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100117161-C-A

72255579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100117208-A-G

72255683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100117292-C-G

72255683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100117292-C-T

72255740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100117355-G-A

72255849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100117457-C-T

72256246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100117753-C-T

http://identifiers.org/hco/3/GRCh38#72256257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100117763-C-A

72256257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100117763-C-T

72256273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100117779-G-A

72256275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100117781-T-C

http://identifiers.org/hco/3/GRCh38#72256283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100117789-C-A

72256448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100117924-C-T

72256663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100118322-T-C

72256674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100118333-G-A

72256969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100118588-G-A

http://identifiers.org/hco/3/GRCh38#72256996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100118613-C-A

72257155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100118773-C-T

72257287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100118898-A-T

72257402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100119002-A-G

72257403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100119003-T-C

72258217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100120449-T-C

72258221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100120453-C-T

72258250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100120480-C-T

72258395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100120578-C-T

72258442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100120614-C-T

http://identifiers.org/hco/3/GRCh38#72258455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100120615-C-A

72258455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100120615-C-T

72258480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100120638-A-G

72258543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100120695-A-G

72258603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100120755-C-T

72258610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100120762-C-T

72258694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100120846-G-A

72258694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100120846-G-T

72258726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100120855-T-C

72259166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100121267-T-A

72259166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100121267-T-C

72259208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100121296-A-G

72259342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100121439-T-C

72259687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100121729-C-T

72260445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100123315-T-C

72260453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100123342-A-T

72260488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100123387-C-G

72260749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100123635-G-T

72260814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100123701-G-C

72260866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100123752-G-A

72262185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100124694-C-T

72262278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100124774-A-G

72263014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100125800-C-T

72263144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100125960-G-A

72263144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100125960-G-C

72263279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100126084-T-A

72263794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100126590-G-A

72263822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100126617-G-A

72264331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100126716-T-C

72264441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100126823-C-G

72264482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100126866-A-T

72264540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100126921-C-T

72264541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100126922-G-A

72264847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100127289-C-G

http://identifiers.org/hco/3/GRCh38#72264915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100127332-C-A

72264963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100127381-T-G

72265214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100127566-C-G

72265214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100127566-C-T

72265395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100127718-C-T

72265606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100127925-A-G

72265755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100128045-C-T

72265794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100128073-G-C

72265823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100128102-C-G

72265823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100128102-C-T

72265832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100128118-G-A

72265912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100128187-C-T

72266158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100128409-C-T

72266202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100128452-A-G

72266213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100128463-A-G

72266218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100128468-G-A

72268732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100130055-T-C

72268785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100130129-C-T

72268901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100130243-T-A

72271123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

72271144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

72271185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

72271297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

72271454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/3/GRCh38#72271685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

72271685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

72271843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

http://identifiers.org/hco/3/GRCh38#72271975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100133849-C-A

72272271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100134131-G-A

72272764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100134552-G-A

http://identifiers.org/hco/3/GRCh38#72272883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100134754-A-C

72272883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100134754-A-G

72273185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100135782-A-G

72273256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100135855-C-G

72273600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100136208-T-A

72273600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100136208-T-C

72273711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100136310-C-T

72273821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100136426-G-A

72273821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100136426-G-C

72274026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100136626-G-T

72274143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100136717-G-T

72274233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100136821-T-A

72274299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100137444-G-A

72274369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100137504-C-T

72274522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100137650-T-C

72274522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100137650-T-G

72274526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100137654-A-G

72274755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100137848-T-C

72274959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100138132-A-T

72275092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100138344-T-C

72275136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: non coding transcript exon variant
orthologous variants: 100138365-T-A

http://identifiers.org/hco/3/GRCh38#72275228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100138443-C-A

72275461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100138651-T-C

72275519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100138709-T-G

72275616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100138774-A-G

72275936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27706
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100139100-G-T