http://identifiers.org/hco/17/GRCh38#12672140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65154445-C-A

12672242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65154355-A-T

12672671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65153921-C-G

12673044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65153575-T-G

12673148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65153468-T-C

12673285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65153338-C-T

http://identifiers.org/hco/17/GRCh38#12673422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65153265-A-C

12673438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65153248-G-A

12673518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65153171-T-A

12673521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65153168-G-A

12673521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65153168-G-T

12673532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65153157-T-G

12673644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65153061-T-C

12673869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65152871-T-C

12674098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65152663-C-G

12674205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65152544-G-C

12674205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65152544-G-T

12674347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65152339-C-T

12674351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65152335-C-T

12674466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65152244-C-T

12674633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65152056-G-A

12674633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65152056-G-T

12674666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65152015-T-C

http://identifiers.org/hco/17/GRCh38#12674885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65151765-A-C

12674976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65151673-T-A

12675199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65151286-A-T

http://identifiers.org/hco/17/GRCh38#12675391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65151012-A-C

12675430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65150973-T-A

12675436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65150967-A-G

12675513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65150911-T-G

12676237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65150376-G-A

12676245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65150368-G-A

12676484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65150155-T-A

12676484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65150155-T-C

12676484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65150155-T-G

12676730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65149952-G-A

http://identifiers.org/hco/17/GRCh38#12678271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65149141-C-A

12678468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65148926-G-A

12678468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65148926-G-T

12678977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65148687-A-G

12678997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65148667-T-A

12679083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65148603-C-G

12679389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65148362-A-G

12679489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65148269-T-C

12679609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65148086-G-A

12679765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65147945-T-C

12679789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65147923-A-G

12680148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65147655-C-T

12680313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65147490-A-G

12680319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65147484-A-G

12680581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65147221-A-G

12680810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65146959-C-T

12681079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65146755-T-C

12681166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65146674-G-A

12681198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65146642-G-A

12681959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65146021-A-G

12681981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145999-G-A

12682018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145970-T-C

12682151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145848-G-A

12682151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145848-G-T

12682189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145810-C-G

12682441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145611-T-C

12682484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145568-T-C

12682492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145560-C-T

12682529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145524-G-A

12682541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145512-A-G

12682573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145481-C-T

12682822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145099-A-T

12682831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145090-C-T

12682876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65145050-C-T

12683123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65144820-G-T

12683869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65144499-A-G

http://identifiers.org/hco/17/GRCh38#12684119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65144105-C-A

12684279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65143950-A-G

12684356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65143906-C-G

http://identifiers.org/hco/17/GRCh38#12684451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65143831-C-A

12684451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65143831-C-T

12684497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65143791-G-A

12684648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65143636-T-C

12685826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65143220-C-T

12685863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65143185-T-C

12686207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65142902-A-G

12686294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65142818-C-T

12687298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65141929-G-A

12687604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65141657-C-T

12687768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65141488-G-A

12687836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65141442-T-C

12687865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65141414-T-A

12687869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65141410-A-G

12687893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65141386-C-T

12687894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65141385-A-G

12688082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65141232-G-C

12688083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65141231-T-C

12688990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65140116-C-T

12689173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65139976-T-C

12689327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65139784-C-G

http://identifiers.org/hco/17/GRCh38#12689328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65139783-C-A

12689353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65139754-C-T

12689391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65139720-G-A

12689486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65139638-A-G

12689828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65139332-C-T

12690093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65138818-A-T

12690198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65138720-G-A

http://identifiers.org/hco/17/GRCh38#12690251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65138663-A-C

12690251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65138663-A-T

12690351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65138566-C-T

12690416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65138549-C-G

12690574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65138412-G-C

12690585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65138401-G-A

12690728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65138108-G-A

12690728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65138108-G-T

12690848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65138005-A-G

12690963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65137909-A-G

12691414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65137472-G-A

12691508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65137363-A-T

12691583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65137288-G-T

12691826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65136854-A-G

12691940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65136740-C-T

12691947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65136733-C-T

http://identifiers.org/hco/17/GRCh38#12691977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65136702-C-A

12692022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65136658-G-A

http://identifiers.org/hco/17/GRCh38#12692175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65136521-A-C

12692253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65136446-T-C

12692302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65136315-C-T

12692320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65136297-G-A

12692328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65136289-G-T

12692351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65136262-A-G

http://identifiers.org/hco/17/GRCh38#12692615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65136026-C-A

12692630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65136011-C-T

12692670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65135971-C-T

12692674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65135967-A-G

12692786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65135889-C-G

12692827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65135886-C-T

http://identifiers.org/hco/17/GRCh38#12692842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65135871-A-C

12693041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65135805-G-A

12693148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65135698-T-G

12693236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65135613-C-G

12693236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65135613-C-T

12693237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65135612-C-G

http://identifiers.org/hco/17/GRCh38#12693313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65135561-A-C

12693385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65135504-G-A

12693394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65135495-G-A

12693862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65135189-G-A

12693875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65135176-G-A

http://identifiers.org/hco/17/GRCh38#12694219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65134713-A-C

12694410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65134537-G-A

12694472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65134474-G-A

12694873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65133047-G-A

12694873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65133047-G-C

12694873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65133047-G-T

http://identifiers.org/hco/17/GRCh38#12694923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65133010-C-A

12694933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65133000-T-A

http://identifiers.org/hco/17/GRCh38#12694998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65132936-A-C

12695030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65132908-A-G

12695030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65132908-A-T

12696538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65131537-G-A

12696542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65131533-A-G

12696827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65131300-C-G

12696992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65131130-C-T

12697258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65130955-A-G

12697365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65130925-T-A

12697365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65130925-T-G

12697373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65130917-T-A

12697653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65130835-A-G

12697817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65130663-C-T

http://identifiers.org/hco/17/GRCh38#12697875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65130608-A-C

12697890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65130593-G-C

12697891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65130592-G-C

12697913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65130572-C-T

12698066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65130339-A-T

12698098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65130307-G-A

http://identifiers.org/hco/17/GRCh38#12698408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65129889-C-A

12698414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65129856-G-C

12698481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65129772-C-G

12698481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65129772-C-T

12700866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65128474-A-G

12700881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65128459-G-A

12704244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124833-G-A

12704244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124833-G-C

12704485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124620-G-A

12704485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124620-G-T

http://identifiers.org/hco/17/GRCh38#12704652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65124465-C-A

12704707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124411-A-G

http://identifiers.org/hco/17/GRCh38#12704709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65124409-C-A

12704764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124357-G-T

http://identifiers.org/hco/17/GRCh38#12704802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65124295-C-A

12704860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124250-G-A

12704860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124250-G-T

12704862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124248-A-G

12704862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124248-A-T

12704863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124247-T-C

12704863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124247-T-G

12704900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124212-C-G

12704965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 65124160-C-G

12704965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 65124160-C-T

12704971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 65124154-T-C

12704986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 65124143-A-G

12704986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 65124143-A-T

http://identifiers.org/hco/17/GRCh38#12705009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65124121-C-A

12705015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124114-A-G

12705066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124068-G-T

12705079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124056-T-C

http://identifiers.org/hco/17/GRCh38#12705105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65124031-A-C

12705105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65124031-A-G

http://identifiers.org/hco/17/GRCh38#12705202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65123934-C-A

12705244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65123896-G-C

12705244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65123896-G-T

http://identifiers.org/hco/17/GRCh38#12705262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65123879-C-A

12705262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65123879-C-T

12705293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65123848-G-A

12705296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65123845-T-A

http://identifiers.org/hco/17/GRCh38#12705358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65123786-C-A

http://identifiers.org/hco/17/GRCh38#12705663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#65123420-A-C

12705663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40750
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 65123420-A-G