7636553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 3 prime UTR variant
orthologous variants: 8255791-A-G

7636579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 3 prime UTR variant
orthologous variants: 8255806-G-C

7636579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 3 prime UTR variant
orthologous variants: 8255806-G-T

http://identifiers.org/hco/7/GRCh38#7636598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8255825-C-A

http://identifiers.org/hco/7/GRCh38#7636605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8255836-C-A

7636605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 3 prime UTR variant
orthologous variants: 8255836-C-T

7636616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 3 prime UTR variant
orthologous variants: 8255847-A-G

http://identifiers.org/hco/7/GRCh38#7636795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8255963-C-A

7636795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 3 prime UTR variant
orthologous variants: 8255963-C-T

7636819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 3 prime UTR variant
orthologous variants: 8255996-A-G

7636835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 3 prime UTR variant
orthologous variants: 8256012-G-A

7636835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 3 prime UTR variant
orthologous variants: 8256012-G-C

7636835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 3 prime UTR variant
orthologous variants: 8256012-G-T

7636942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 3 prime UTR variant
orthologous variants: 8256108-G-T

http://identifiers.org/hco/7/GRCh38#7637023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8256188-A-C

7637128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8256292-G-T

7637289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8256427-C-T

7637894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8256725-C-T

7638026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8256856-T-G

7638101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8256954-T-A

7638101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8256954-T-G

7638154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8256988-T-A

7638154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8256988-T-C

7638154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8256988-T-G

7638204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8257040-T-C

http://identifiers.org/hco/7/GRCh38#7638206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8257042-C-A

7638206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8257042-C-T

http://identifiers.org/hco/7/GRCh38#7638225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8257061-C-A

7638225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8257061-C-T

http://identifiers.org/hco/7/GRCh38#7638297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8257151-C-A

7638297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8257151-C-G

7638350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8257201-T-A

7638895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8257540-T-C

7638927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8257574-A-G

7638927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8257574-A-T

7638928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8257575-G-A

7638928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8257575-G-C

7638928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8257575-G-T

7639038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8257658-T-C

7639150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8257767-A-G

http://identifiers.org/hco/7/GRCh38#7639158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8257775-A-C

7639158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8257775-A-G

7639686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258401-G-A

http://identifiers.org/hco/7/GRCh38#7639833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8258538-C-A

7639833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258538-C-T

7639845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258550-A-G

7639845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258550-A-T

7639862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258566-C-T

http://identifiers.org/hco/7/GRCh38#7639912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8258616-C-A

7639912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8258616-C-G

7639912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8258616-C-T

http://identifiers.org/hco/7/GRCh38#7639942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8258648-A-C

7639942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8258648-A-G

7640001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8258687-T-A

7640001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8258687-T-C

http://identifiers.org/hco/7/GRCh38#7640020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8258706-C-A

7640020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8258706-C-G

7640020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8258706-C-T

7640061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8258748-G-A

http://identifiers.org/hco/7/GRCh38#7640086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8258769-C-A

7640086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258769-C-G

7640086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258769-C-T

7640096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258779-A-G

7640109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258789-G-A

7640109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258789-G-C

7640109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258789-G-T

7640114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258794-T-C

http://identifiers.org/hco/7/GRCh38#7640136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8258812-C-A

7640136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258812-C-T

7640166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258846-G-A

7640166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258846-G-T

http://identifiers.org/hco/7/GRCh38#7640231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8258921-C-A

7640231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258921-C-T

7640254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258946-G-A

7640254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258946-G-T

7640275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8258976-C-G

7640275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8258976-C-T

7640314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8258992-G-A

7640364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 8259044-G-A

7640366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259046-G-A

7640366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259046-G-C

http://identifiers.org/hco/7/GRCh38#7640367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8259047-C-A

7640367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259047-C-G

7640367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259047-C-T

http://identifiers.org/hco/7/GRCh38#7640389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8259069-C-A

7640389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 8259069-C-T

7640397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259077-G-A

7640397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259077-G-C

7640427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259108-T-G

7640432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259113-G-A

7640432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259113-G-C

7640474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259149-G-A

7640474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259149-G-T

7640483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259158-G-A

7640483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259158-G-C

7640483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259158-G-T

7640497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259179-G-A

7640497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259179-G-T

http://identifiers.org/hco/7/GRCh38#7640566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#8259251-C-A

7640566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259251-C-T

7640571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259254-T-A

7640571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8259254-T-G

7640609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8259282-G-A

7640609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8259282-G-T

7640672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259350-G-A

7640672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259350-G-C

7640672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259350-G-T

http://identifiers.org/hco/7/GRCh38#7640674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8259352-C-A

7640674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259352-C-T

7640792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 8259465-T-C

7640792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 8259465-T-G

http://identifiers.org/hco/7/GRCh38#7640861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8259532-C-A

7640861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259532-C-T

7640921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259596-C-T

7641009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259646-C-T

7641051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259689-C-T

7641171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259776-T-C

7641271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259863-C-T

http://identifiers.org/hco/7/GRCh38#7641275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8259867-C-A

7641275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259867-C-G

7641275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259867-C-T

7641308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8259891-G-C

7641481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8260039-T-C

7641548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8260075-C-G

7641548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8260075-C-T

7641573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8260085-G-C

7641583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8260095-T-C

7641618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8260128-A-G

7641618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8260128-A-T

7641674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8260216-A-G

7641682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8260224-T-C

7641739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8260281-G-A

7641739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8260281-G-T

http://identifiers.org/hco/7/GRCh38#7641847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8260436-C-A

7641905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8260498-C-T

7663958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8267270-T-C

7664280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8267655-C-G

7664689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8268084-G-A

7664911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8268286-G-A

7664913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8268288-T-C

7664922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8268297-G-A

7664976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8268350-A-G

7665021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8268386-A-T

7665259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8268597-A-G

7672045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8269689-A-G

7672075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8269718-T-G

7672100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8269742-A-G

http://identifiers.org/hco/7/GRCh38#7673164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8270332-C-A

7673206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8270374-A-G

7673247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8270414-A-T

7673298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8270462-T-C

7673329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 8270493-A-G

7673422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 8270550-A-G

7673486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8270615-G-T

7673491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8270620-A-G

7673544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8270665-C-T

7675179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8270994-T-C

7675221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8271033-G-C

7675400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8271191-C-T

7675407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8271198-C-G

7675407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8271198-C-T

7675470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8271261-C-G

http://identifiers.org/hco/7/GRCh38#7675614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8271399-A-C

7675647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8271430-C-T

7675724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8271561-A-G

http://identifiers.org/hco/7/GRCh38#7675757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8271594-A-C

7675757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8271594-A-G

7675809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8271645-G-T

7676095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 8271918-T-A

http://identifiers.org/hco/7/GRCh38#7676096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8271919-C-A

7676096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 8271919-C-T

7676109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 8271932-T-C

7676116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 8271939-C-T

7676159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 8271982-C-T

7676165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 8271985-G-C

http://identifiers.org/hco/7/GRCh38#7676180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8271994-C-A

7676264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8272045-G-A

7676324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8272083-A-G

7676337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8272096-G-A

7676337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8272096-G-T

7676354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8272108-T-C

7676585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8273888-A-G

http://identifiers.org/hco/7/GRCh38#7676673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8273966-C-A

7676713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8274005-T-C

7676783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8274072-A-G

7676856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8274142-A-G

7676906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8274178-T-C

7677067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8274333-C-G

7677073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8274339-C-G

7680962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8274678-G-C

7681058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8274773-A-T

7681277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8274975-G-C

7681277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8274975-G-T

7681299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8274983-G-C

7681398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8275035-G-C

7681599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8275231-T-C

7681701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8275332-T-A

7682088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8275693-A-T

7682105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8275710-T-G

7682468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8276025-C-T

7682480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8276063-G-A

7682485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8276068-C-T

7682707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8276280-T-C

7682737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8276297-C-G

7682737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8276297-C-T

7682939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8276479-C-G

7686164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8276613-A-G

7686192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8276641-G-A

7686486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8276889-A-T

7686690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8277055-A-G

7686763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8277133-C-T

7686912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8277426-C-T

7686913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8277427-C-G

7687063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8277591-A-T

7687131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8277662-C-T

7687189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8277722-G-T

7687235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8277806-G-T

7687237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8277808-C-T

7687269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8277889-A-G

http://identifiers.org/hco/7/GRCh38#7687307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8277947-C-A

7687390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8278078-G-A

7687416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8278103-A-G

http://identifiers.org/hco/7/GRCh38#7687422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8278109-C-A

7687422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8278109-C-T

7687509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8278283-A-G

7687515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8278289-C-T

7687528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8278307-A-G

7687812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8278828-T-C

7687883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8278894-G-A

7688163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8279146-T-C

http://identifiers.org/hco/7/GRCh38#7688274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8279263-C-A

7690530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8279772-G-T

7690711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8279963-A-G

7690880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8280139-C-G

7690880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8280139-C-T

7690911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8280169-T-A

7691026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8280284-C-G

7691204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8280454-G-T

7691243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8280494-A-G

7691403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8280689-T-C

7691454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8280731-A-G

7691599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8280858-T-C

7691611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8280868-A-G

7692975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8283514-A-G

7693004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8283543-A-T

7693011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8283550-T-C

7693510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8283804-T-C

7694111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8285319-T-C

7694156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8285360-G-A

7695210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8285379-G-A

7695593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8285750-A-G

7695844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8285925-G-A

7695898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8285970-C-G

7696655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8287129-A-G

7696769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8287265-T-C

7696913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8287386-C-G

7696913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8287386-C-T

7696965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8287437-T-C

7697164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8287623-T-A

7697639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8288090-T-C

7697660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8288115-A-G

7697965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8288406-C-T

7697997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8288432-C-T

7702285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8289180-T-G

7702397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8289258-A-G

7702397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8289258-A-T

7702401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8289263-A-G

7702401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8289263-A-T

7702470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8289329-C-G

7702965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8289505-G-A

7702965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8289505-G-C

7702965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8289505-G-T

7703069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8289607-T-C

7703257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8289795-A-G

7706473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8292816-C-T

7706519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8292872-A-G

7706774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8293078-A-G

7706816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8293113-A-G

7707360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8293598-G-A

7707420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8293656-C-G

7707426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8293662-T-C

7707460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8293696-C-T

7707617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8293843-A-G

7707706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8293936-C-G

7707706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8293936-C-T

7708390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8294663-A-G

7708486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8294751-A-G

7709120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8295313-C-T

7709225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8295421-G-C

7709225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8295421-G-T

7709421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8295595-T-G

7709525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8295683-G-A

7709562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8295719-A-G

http://identifiers.org/hco/7/GRCh38#7709818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8296119-A-C

7709818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8296119-A-G

7717529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8297473-A-G

7717749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8297675-A-G

7717768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8297694-C-G

http://identifiers.org/hco/7/GRCh38#7718208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#8298172-A-C

7718404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8298289-C-G

7718404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8298289-C-T

7718484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10291
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8298373-A-G