17042556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 5 prime UTR variant
orthologous variants: 59553397-G-T

17043007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59553811-T-C

17043007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59553811-T-G

http://identifiers.org/hco/17/GRCh38#17043021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59553823-C-A

17043021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59553823-C-T

17043119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59553930-G-A

17043119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59553930-G-T

17043559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59554386-G-T

17043687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59554568-G-A

17043870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59554734-C-G

17043870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59554734-C-T

17044349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59555167-T-A

17044514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59555276-A-G

17044518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59555279-T-C

http://identifiers.org/hco/17/GRCh38#17044563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59555322-A-C

17044563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59555322-A-T

17045184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59555958-G-A

17045697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59556387-G-A

17045997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59556603-A-G

17046316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59556862-T-G

17048302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59559120-G-A

17048349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59559148-G-A

17048432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59559227-T-C

17048759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59559561-G-A

17048982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59559741-C-T

17050832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59560973-G-T

17050902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59561091-T-C

17050921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59561110-C-G

17050921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59561110-C-T

17051324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59561629-C-T

17051508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59561788-A-G

17051826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59562091-A-G

17051917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59562151-G-A

17052520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59562639-G-C

17052733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59562814-C-G

17052733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59562814-C-T

17052981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59563050-G-A

17052981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59563050-G-T

17053107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59563170-C-T

17053248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59563316-A-G

17053248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59563316-A-T

17053484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59563542-A-G

17055443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59564795-G-A

17055632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59564904-T-A

17055912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59565176-G-T

17056207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59565750-G-A

17056244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59565786-G-A

17056284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59565828-G-A

17056284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59565828-G-T

17056644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59566107-A-T

17056723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59566181-T-C

17056789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59566242-T-A

17057017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59566503-T-A

17057336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59566758-G-A

17057336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59566758-G-C

17057443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59566873-G-A

17060217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59569971-G-A

17060529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59570210-G-A

17060551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59570230-A-G

17061055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59571068-G-A

17061177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59571189-C-T

17061181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59571194-C-G

17061285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59571277-G-A

17061306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59571297-G-A

17061641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59571566-G-T

17061763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59571654-G-A

17061956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59571812-G-A

17072982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59584850-A-G

17073154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59584985-T-C

17073956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59585663-C-T

17074654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59585856-C-T

17074797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59585995-T-C

17075121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59586390-T-C

17075563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59586836-G-A

17075563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59586836-G-C

17075563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59586836-G-T

17075691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59586933-C-T

http://identifiers.org/hco/17/GRCh38#17075796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59587038-A-C

17075865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59587110-G-A

17075865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59587110-G-C

17075865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59587110-G-T

http://identifiers.org/hco/17/GRCh38#17075920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59587168-C-A

17077468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59587287-T-G

http://identifiers.org/hco/17/GRCh38#17077490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59587309-C-A

17077689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59587485-C-T

17077723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59587519-G-T

17077861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59587643-G-T

17077914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59587696-C-T

17078103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59587878-G-A

http://identifiers.org/hco/17/GRCh38#17078105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59587880-C-A

17078105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59587880-C-T

17078125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59587900-C-T

17078984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59588630-G-T

17079484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59589083-G-C

17079613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59589180-A-G

17080602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59590529-G-C

17080994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59590810-A-T

http://identifiers.org/hco/17/GRCh38#17081022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59590830-A-C

17081022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59590830-A-G

17081252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59591101-G-C

17081260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59591110-C-T

17081533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59591301-A-G

17081822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59591489-G-A

17081880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59591534-A-G

17081928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59591578-C-T

17088117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59593770-T-C

17088387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59594015-A-G

17095513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59595910-C-T

17095514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59595911-A-G

17096119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59596312-C-T

17096388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59596512-C-T

17096523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59596601-G-T

17096647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59596706-G-A

17096685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59596742-T-C

17096711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59596766-C-T

http://identifiers.org/hco/17/GRCh38#17096737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59596793-C-A

17096965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59597023-T-C

17096977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59597039-A-G

17097027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59597107-G-T

http://identifiers.org/hco/17/GRCh38#17097046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59597129-C-A

17097111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59597219-G-A

17097111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59597219-G-T

http://identifiers.org/hco/17/GRCh38#17097211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59597323-A-C

17097211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59597323-A-G

17097220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59597355-G-A

17097220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59597355-G-T

17097268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59597403-A-T

17097287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59597449-T-C

17098393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59598508-C-T

17098473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59598593-C-G

17098474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59598594-A-G

17098528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59598647-G-T

17098632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59598776-C-T

17098671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59598814-G-A

17099003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59599165-G-A

17099079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59599245-G-C

17099079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59599245-G-T

17099150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59599328-T-C

17100101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59600170-C-T

17100131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59600199-T-G

http://identifiers.org/hco/17/GRCh38#17100277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59600327-A-C

http://identifiers.org/hco/17/GRCh38#17101752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59600980-C-A

17102978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59601485-G-T

17103051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59601557-C-T

17103206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59601708-G-A

17103206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59601708-G-C

17103304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59601935-C-G

17103592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59602189-C-T

http://identifiers.org/hco/17/GRCh38#17108382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59606388-A-C

17108513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59606520-T-G

17114159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59611168-C-T

17114192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59611203-G-A

17114257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59611260-T-C

17114360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59611389-A-G

17114517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59611542-T-C

17114686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59611684-C-T

17114985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59611947-T-C

17120244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59613170-G-A

17120341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59613298-G-A

17120427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59613385-G-A

17120430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59613388-C-T

17124051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59616411-C-T

17124251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59616563-G-A

17124710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59616913-A-G

17124910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59617073-C-T

17124983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59617096-G-C

17124987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59617100-G-A

17125137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59617231-C-T

17125274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59617326-G-A

17125452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59617407-C-G

17125473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59617415-C-T

17126286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59617999-G-C

17126545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59618254-C-T

http://identifiers.org/hco/17/GRCh38#17126550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59618259-A-C

17126550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59618259-A-G

17126588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59618302-G-C

17126588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59618302-G-T

17126590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59618304-G-A

http://identifiers.org/hco/17/GRCh38#17127648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59618848-C-A

17127723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59618911-A-G

17128369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59619446-C-T

17128584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59619648-C-T

17128613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59619688-C-G

17128724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59619890-G-A

17128914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59620058-C-G

17128914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59620058-C-T

17129203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59620245-T-G

17129595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59620638-C-T

17130150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59621143-C-T

17130165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59621158-C-T

17130171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59621164-C-T

http://identifiers.org/hco/17/GRCh38#17130293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59621266-C-A

17131713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59622430-G-A

http://identifiers.org/hco/17/GRCh38#17131796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59622490-C-A

17131796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59622490-C-G

17131796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59622490-C-T

http://identifiers.org/hco/17/GRCh38#17131978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59622677-C-A

17132198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59622846-G-C

17132714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59623376-C-G

17132881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59623567-C-T

17133189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59623868-G-A

17133189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59623868-G-T

17135467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59625538-G-A

17135574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59625619-G-A

17135996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59626321-C-G

17136105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59626547-C-G

17136302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59626742-C-G

17136302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59626742-C-T

http://identifiers.org/hco/17/GRCh38#17136419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59626859-C-A

17136419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59626859-C-T

17136436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59626876-T-C

17136438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59626878-G-A

17136456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59626896-C-T

17136464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59626915-A-G

17136464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59626915-A-T

17136474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59626925-G-A

17136474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59626925-G-T

17136476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59626944-A-G

17136476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59626944-A-T

17136480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59626948-A-G

17137728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59627725-A-G

http://identifiers.org/hco/17/GRCh38#17137805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59627799-A-C

17137805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59627799-A-G

17137805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59627799-A-T

17137808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59627802-T-G

http://identifiers.org/hco/17/GRCh38#17137819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59627815-C-A

17137819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59627815-C-G

17137819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59627815-C-T

17137822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59627818-G-A

17137822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59627818-G-C

17137822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59627818-G-T

http://identifiers.org/hco/17/GRCh38#17138149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59628128-C-A

17138149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 59628128-C-T

17138187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59628166-G-A

17138187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59628166-G-T

17138192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59628171-G-A

17138192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59628171-G-T

http://identifiers.org/hco/17/GRCh38#17138197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59628176-C-A

17138197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59628176-C-T

17138202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59628181-T-C

17138202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59628181-T-G

17138559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59628479-G-T

17138680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59628570-A-G

17138816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59628688-A-G

17139135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59628907-G-A

17139135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59628907-G-T

17139419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59629103-G-A

17139517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59629189-T-A

17140263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59629752-C-G

17140530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59630003-C-T

17140767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59630235-T-C

17140978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59630362-C-T

17141329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59630709-G-A

17141432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59630788-G-A

17141432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59630788-G-C

17141432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59630788-G-T

17141448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59630797-A-G

17141449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59630798-G-A

17141449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59630798-G-C

17141449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59630798-G-T

http://identifiers.org/hco/17/GRCh38#17141452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59630801-A-C

17141452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59630801-A-G

17141452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59630801-A-T

http://identifiers.org/hco/17/GRCh38#17141567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59630884-C-A

17141567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59630884-C-T

17141581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59630895-T-C

http://identifiers.org/hco/17/GRCh38#17141749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59631040-C-A

17141749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59631040-C-T

17142105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59631420-A-G

17142105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59631420-A-T

17142213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59631517-G-T

17142311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59631606-T-C

17142343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59631637-G-A

17142343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59631637-G-T

17142388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59631666-T-C

http://identifiers.org/hco/17/GRCh38#17142451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59631720-C-A

17142451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59631720-C-T

http://identifiers.org/hco/17/GRCh38#17142523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59631811-A-C

17142523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59631811-A-G

17142523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59631811-A-T

http://identifiers.org/hco/17/GRCh38#17142532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59631825-A-C

17142532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59631825-A-G

17142532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59631825-A-T

http://identifiers.org/hco/17/GRCh38#17142535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59631828-C-A

17142535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59631828-C-T

17142540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59631836-G-A

17142702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: synonymous variant
orthologous variants: 59632024-G-A

17142817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59632148-G-A

http://identifiers.org/hco/17/GRCh38#17142826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59632157-C-A

17142826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59632157-C-T

http://identifiers.org/hco/17/GRCh38#17142893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59632216-C-A

17142893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59632216-C-T

17142894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59632217-T-A

17143095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59632420-G-A

17143434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59632715-T-A

17143434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59632715-T-C

17143434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59632715-T-G

http://identifiers.org/hco/17/GRCh38#17143435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59632716-C-A

17143435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59632716-C-T

http://identifiers.org/hco/17/GRCh38#17143763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59633030-C-A

17143763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59633030-C-T

17145078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59633745-G-A

17145333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59633960-G-A

17145591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59634195-G-A

17145591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59634195-G-T

17145851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59634439-G-A

http://identifiers.org/hco/17/GRCh38#17145917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59634473-C-A

17146110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59634671-C-T

17146173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59634701-G-A

17146173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59634701-G-T

17146390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59634794-G-A

17146720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59635040-T-C

17146720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59635040-T-G

17146859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59635175-C-T

17147231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59635493-A-T

http://identifiers.org/hco/17/GRCh38#17147236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59635498-C-A

17147257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59635515-G-A

17147257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59635515-G-C

17147257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59635515-G-T

http://identifiers.org/hco/17/GRCh38#17147271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59635533-C-A

17147273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59635535-G-A

17147273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59635535-G-C

17147284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59635545-G-A

17147284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59635545-G-T

17147365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: missense variant
orthologous variants: 59635624-A-G

17149843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59639133-A-G

17149944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59639225-A-G

17149962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59639243-G-A

17150082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59639314-G-C

17150082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59639314-G-T

17150337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59639507-G-A

17150337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59639507-G-T

http://identifiers.org/hco/17/GRCh38#17150338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#59639508-C-A

17150338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59639508-C-G

17150338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59639508-C-T

17150355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59639525-T-A

17150362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59639532-T-A

http://identifiers.org/hco/17/GRCh38#17150363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59639533-C-A

17150363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59639533-C-G

http://identifiers.org/hco/17/GRCh38#17150380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59639550-C-A

17150380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59639550-C-T

17150483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59639660-T-A

17150556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59639730-A-G

17154177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59640232-A-G

17154258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59640298-G-A

17154393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59640432-A-T

17156876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59642321-G-A

17156992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59642415-C-T

17158036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59643000-C-T

17158292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59643218-A-G

17158295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59643221-T-C

17158295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59643221-T-G

http://identifiers.org/hco/17/GRCh38#17158487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59643368-C-A

http://identifiers.org/hco/17/GRCh38#17158600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59643481-C-A

17158609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59643490-C-T

17158640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59643521-G-A

17158640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59643521-G-T

17158776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59643657-C-T

17158804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59643685-G-A

17158912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59643796-G-A

17160805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59645467-G-C

17160861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59645512-C-G

17160861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59645512-C-T

17160872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59645523-A-G

http://identifiers.org/hco/17/GRCh38#17161150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59645728-C-A

17161366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59645944-A-G

http://identifiers.org/hco/17/GRCh38#17161391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59645968-C-A

17161391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59645968-C-T

17161617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59646154-A-G

17161780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59646310-A-T

http://identifiers.org/hco/17/GRCh38#17161841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59646405-A-C

17162072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59646646-G-A

17162197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59646771-G-A

17162243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59646810-A-G

17162693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59647265-G-A

17163308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59647614-C-G

17163939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59648173-A-G

17163987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59648227-G-A

17163987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59648227-G-T

17164269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59648510-G-A

17164279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59648520-G-A

http://identifiers.org/hco/17/GRCh38#17164294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59648535-C-A

17164381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59648622-G-C

17164381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59648622-G-T

http://identifiers.org/hco/17/GRCh38#17164835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59649076-C-A

17164835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59649076-C-T

17164963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59649204-C-T

17165026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59649267-G-T

17165117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59649358-G-A

17165117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59649358-G-C

17165278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59649519-G-A

17165377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59649612-G-C

17165791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59650017-G-A

17165791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59650017-G-T

17166277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59650503-G-T

17166425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59650669-G-A

17166976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59651208-G-A

17167612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59651847-G-A

http://identifiers.org/hco/17/GRCh38#17167841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59652079-C-A

http://identifiers.org/hco/17/GRCh38#17167909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59652147-C-A

17167909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59652147-C-G

17167909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59652147-C-T

17167988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59652222-A-G

17167988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59652222-A-T

http://identifiers.org/hco/17/GRCh38#17168073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59652297-C-A

17168073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59652297-C-T

http://identifiers.org/hco/17/GRCh38#17168233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59652393-A-C

17168233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59652393-A-G

17168233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59652393-A-T

17168976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59652911-G-T

17169006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59652943-G-A

http://identifiers.org/hco/17/GRCh38#17169088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59653008-C-A

17169134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59653054-G-T

17170479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59654374-C-T

17170527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59654425-G-T

17170556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59654454-A-G

17170608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59654502-C-T

17170734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59654579-T-C

17170955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59654745-C-G

17170955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59654745-C-T

http://identifiers.org/hco/17/GRCh38#17171073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59654862-A-C

17171073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59654862-A-T

17171648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59655137-C-G

17171648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59655137-C-T

17171676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59655168-G-A

17172085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59655554-C-G

17172166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59655657-C-G

17172236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59655773-G-A

http://identifiers.org/hco/17/GRCh38#17172325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59655891-C-A

17172331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59655897-C-T

17172570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656093-A-G

17172570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656093-A-T

17172588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656107-A-G

17172588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656107-A-T

http://identifiers.org/hco/17/GRCh38#17172597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59656116-C-A

17172597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656116-C-G

17172597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656116-C-T

http://identifiers.org/hco/17/GRCh38#17172881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59656409-C-A

17172881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656409-C-T

http://identifiers.org/hco/17/GRCh38#17172941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59656452-C-A

17172941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656452-C-G

17172941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656452-C-T

17173304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656812-T-C

17173525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59657128-G-A

17173774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59657450-C-G

17173774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59657450-C-T

17173872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59657509-T-C

17173973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59657611-G-A

17175260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59658743-C-G

17175260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59658743-C-T

http://identifiers.org/hco/17/GRCh38#17175474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59659011-C-A

17175474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59659011-C-T

17175704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59659283-A-G

17176285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59659896-G-A

17176285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59659896-G-C

17176285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59659896-G-T

17176328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59659939-G-A

17176328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59659939-G-C

17176328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59659939-G-T

17176344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59659958-T-A

17176458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59660071-G-A

17176711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59660305-T-C

17176740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59660330-A-G

17176899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59660483-T-C

17177132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59660644-T-G

http://identifiers.org/hco/17/GRCh38#17177139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59660651-C-A

http://identifiers.org/hco/17/GRCh38#17177427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59660885-C-A

17177542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59660961-G-A

17177542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59660961-G-T

http://identifiers.org/hco/17/GRCh38#17179617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59662157-C-A

17179617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59662157-C-G

17179617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59662157-C-T

17179618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59662158-T-C

17179670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59662202-G-A

http://identifiers.org/hco/17/GRCh38#17179679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59662212-C-A

17179679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59662212-C-T

17179740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59662274-G-A

17180100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59662538-G-T

17180217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59662624-C-T

17180259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59662666-T-C

http://identifiers.org/hco/17/GRCh38#17180276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59662687-C-A

17180498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59662868-G-A

17180498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59662868-G-C

17180728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59663122-T-C

17180932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59663294-A-G

17184037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59665717-C-T

17184157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59665841-C-T

http://identifiers.org/hco/17/GRCh38#17184158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59665842-A-C

17184158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59665842-A-G

17184378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59665955-T-C

17184450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59666012-G-A

17184501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59666060-T-C

http://identifiers.org/hco/17/GRCh38#17184673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59666216-A-C

http://identifiers.org/hco/17/GRCh38#17184690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59666244-C-A

17184690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59666244-C-T

http://identifiers.org/hco/17/GRCh38#17184709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59666267-C-A

17184709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59666267-C-G

17184968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59666481-G-A

17184968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59666481-G-C

http://identifiers.org/hco/17/GRCh38#17184971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59666484-C-A

17184971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59666484-C-T

http://identifiers.org/hco/17/GRCh38#17185026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59666520-C-A

17185026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59666520-C-G

http://identifiers.org/hco/17/GRCh38#17185066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59666559-C-A

17185066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59666559-C-G

http://identifiers.org/hco/17/GRCh38#17185150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59666653-A-C

17185150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59666653-A-G

17185150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59666653-A-T

17185702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59667167-G-T

17186000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59667404-A-G

17191549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59670739-C-T

http://identifiers.org/hco/17/GRCh38#17191570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59670760-C-A

17191570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59670760-C-T

http://identifiers.org/hco/17/GRCh38#17191595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59670798-C-A

17191595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59670798-C-T

http://identifiers.org/hco/17/GRCh38#17191605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59670808-C-A

17191605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59670808-C-T

17191637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59670838-C-T

http://identifiers.org/hco/17/GRCh38#17191701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59670883-C-A

17191701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59670883-C-T

http://identifiers.org/hco/17/GRCh38#17191704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59670886-C-A

http://identifiers.org/hco/17/GRCh38#17191768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59670949-C-A

17191768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59670949-C-T

17191932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59671099-T-A

17192011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59671182-T-A

17192117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59671240-T-A

http://identifiers.org/hco/17/GRCh38#17192253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59671328-C-A

17192253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59671328-C-G

17202950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 59675903-G-A

17202950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59675903-G-C

17202950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59675903-G-T

17203103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 59676056-A-G

17203154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59676105-A-G

17203168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59676119-C-G

17203168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59676119-C-T

17203171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59676122-C-G

17203171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59676122-C-T

17206007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59678191-G-A

17206007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59678191-G-C

17206007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59678191-G-T

17206175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59678353-G-A

17206175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59678353-G-T

http://identifiers.org/hco/17/GRCh38#17206189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#59678364-C-A

17206189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 59678364-C-T

http://identifiers.org/hco/17/GRCh38#17206254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59678429-C-A

17206254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59678429-C-G

17206254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59678429-C-T

http://identifiers.org/hco/17/GRCh38#17206306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#59678485-C-A

17206306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 59678485-C-T

17206338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59678524-G-A

17206338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59678524-G-T

17206359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59678541-G-A

17206359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59678541-G-C

http://identifiers.org/hco/17/GRCh38#17206402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#59678585-C-A

17206402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, undefined
orthologous variants: 59678585-C-G

http://identifiers.org/hco/17/GRCh38#17212167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59682530-C-A

http://identifiers.org/hco/17/GRCh38#17212341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59682707-A-C

17212349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59682715-T-C

17212466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59682792-C-T

17212547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59682866-G-A

17212547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59682866-G-T

17212573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59682892-T-C

17213596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59683393-C-T

17213651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 59683432-C-T

17213691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59683472-C-G

17213691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59683472-C-T

17213716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59683497-G-A

17213716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant
orthologous variants: 59683497-G-T

17213775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59683556-A-G

17213841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59683622-A-T

17213867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59683648-C-G

http://identifiers.org/hco/17/GRCh38#17213980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59683767-C-A

17213980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59683767-C-T

17213989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59683776-T-G

17213992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59683779-G-A

17213992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59683779-G-T

17214056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59683926-G-A

17214056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59683926-G-C

17214121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59684008-A-G

17214318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59684230-A-G

17214332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59684246-A-G

http://identifiers.org/hco/17/GRCh38#17214878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59684853-C-A

17214878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59684853-C-T

17215111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685039-A-G

17215291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 59685205-G-A

17215312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 59685226-A-G

17215372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685275-T-C

17215373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685276-G-C

17215373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685276-G-T

17215374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685277-C-T

17215385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685287-C-T

17215406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685299-C-T

17215486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685365-G-A

17215486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685365-G-C

17215666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685464-C-T

http://identifiers.org/hco/17/GRCh38#17216238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59685814-A-C

17216238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685814-A-G

http://identifiers.org/hco/17/GRCh38#17216241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59685817-C-A

17216253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685829-G-A

17216253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685829-G-C

17216253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685829-G-T

17216259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685850-G-T

http://identifiers.org/hco/17/GRCh38#17216281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59685873-C-A

17216281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685873-C-T

17216300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685892-G-C

17216305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685897-C-G

http://identifiers.org/hco/17/GRCh38#17216328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59685920-C-A

17216328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59685920-C-T

17216459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 59686046-G-A

17216637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59686172-A-G

17216637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59686172-A-T

17216638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron variant
orthologous variants: 59686173-G-A

17216979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59686514-G-A

17216979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59686514-G-T

http://identifiers.org/hco/17/GRCh38#17216981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59686516-A-C

17216981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59686516-A-G

17216981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59686516-A-T

17216996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59686530-G-A

17216996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59686530-G-T

17216997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59686531-C-G

17216997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59686531-C-T

17217049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59686559-T-C

http://identifiers.org/hco/17/GRCh38#17217050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59686560-A-C

17217050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59686560-A-G

http://identifiers.org/hco/17/GRCh38#17217070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59686577-C-A

17217070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 59686577-C-T

17217250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59686756-G-A

17217250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59686756-G-T

http://identifiers.org/hco/17/GRCh38#17217282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#59686786-A-C

17217327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59686828-G-A

17217356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59686853-G-A

17217356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59686853-G-C

17217356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59686853-G-T

17217370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59686871-G-A

17217370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59686871-G-C

17217370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30321
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59686871-G-T