http://identifiers.org/hco/12/GRCh38#56118383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128383496-C-A

56118383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128383496-C-T

56118437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128383432-T-C

56118603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128383276-C-T

56118678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128383206-G-A

56118678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128383206-G-T

56118734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128383148-A-G

http://identifiers.org/hco/12/GRCh38#56118738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128383144-C-A

56118738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128383144-C-T

http://identifiers.org/hco/12/GRCh38#56118916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128382951-C-A

56118916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128382951-C-T

http://identifiers.org/hco/12/GRCh38#56118937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128382930-C-A

56118942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 128382925-G-T

56119286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128382560-T-G

http://identifiers.org/hco/12/GRCh38#56119464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128382443-C-A

http://identifiers.org/hco/12/GRCh38#56119549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128382358-C-A

56119549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128382358-C-T

http://identifiers.org/hco/12/GRCh38#56120016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128381927-C-A

56120020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128381923-C-T

56120071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 128381868-G-A

56120071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 128381868-G-T

56120198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128381741-T-G

56120292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128381620-T-C

56120373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128381539-G-A

56120373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128381539-G-C

56120373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128381539-G-T

56120514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128381405-T-C

56120592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128381324-T-C

56120598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128381318-G-A

56120598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 128381318-G-C

56120621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 128381295-G-T

http://identifiers.org/hco/12/GRCh38#56120636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128381280-A-C

56120944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128380972-G-T

56121424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 128380489-G-C

http://identifiers.org/hco/12/GRCh38#56121844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128380069-C-A

56121844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 128380069-C-G

56121844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 128380069-C-T

56121915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128379994-A-G

56121933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128379976-C-T

56122053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128379848-G-T

56122060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128379841-C-T

http://identifiers.org/hco/12/GRCh38#56122097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128379808-A-C

56122097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128379808-A-G

56122097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128379808-A-T

56122108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128379797-C-G

http://identifiers.org/hco/12/GRCh38#56122114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128379791-C-A

56122114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128379791-C-T

56122142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128379767-G-A

56122142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128379767-G-T

56122510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128379425-A-G

http://identifiers.org/hco/12/GRCh38#56122581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128379356-C-A

56122581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128379356-C-T

56122624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128379325-A-G

56122624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128379325-A-T

56123080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128378757-A-G

56123158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128378703-G-A

56123191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128378691-G-A

56123191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128378691-G-T

56123254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128378641-T-C

56123261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128378634-T-C

56123305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128378585-A-G

http://identifiers.org/hco/12/GRCh38#56126191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#128372424-C-A

http://identifiers.org/hco/12/GRCh38#56126277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#128372362-C-A

http://identifiers.org/hco/12/GRCh38#56126295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#128372345-C-A

56126295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128372345-C-T

56126590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128372087-T-C

56127527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128362422-T-C

56127573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128362377-G-T

56127635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128362319-C-T

56127647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128362294-G-T

56127660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128362281-A-T

56127946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128362002-T-A

56127946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128362002-T-C

56127946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128362002-T-G

56128024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128361927-T-C

56128024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128361927-T-G

56128043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128361906-T-C

http://identifiers.org/hco/12/GRCh38#56128063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128361887-C-A

56128063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128361887-C-T

56128366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 128361644-A-G

http://identifiers.org/hco/12/GRCh38#56128659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128361381-C-A

http://identifiers.org/hco/12/GRCh38#56128718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128361322-C-A

56128718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128361322-C-T

56128768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128361274-G-A

56128768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128361274-G-T

http://identifiers.org/hco/12/GRCh38#56128804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128361242-C-A

56128804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128361242-C-T

56128815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128361231-T-C

http://identifiers.org/hco/12/GRCh38#56128871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128361177-C-A

56128871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128361177-C-G

56129149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128360906-T-C

http://identifiers.org/hco/12/GRCh38#56129195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128360861-C-A

56129195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128360861-C-T

http://identifiers.org/hco/12/GRCh38#56129227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#128360804-C-A

http://identifiers.org/hco/12/GRCh38#56129286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128360764-C-A

56129286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128360764-C-G

56129286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128360764-C-T

56129316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128360728-G-T

http://identifiers.org/hco/12/GRCh38#56129544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128360495-C-A

56129544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128360495-C-T

http://identifiers.org/hco/12/GRCh38#56129656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128360418-C-A

56130278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128360074-A-G

56130344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128360000-T-G

56130384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128359959-A-G

56130401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128359942-A-G

56130415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128359926-A-G

56130477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128359083-G-A

56130648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128358910-C-T

56130674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128358893-T-G

56130964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128358261-G-A

56131061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128358168-A-G

56131322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128357916-C-T

56131394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128357846-G-A

56131394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128357846-G-C

56131513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128357747-A-G

56131585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128357676-G-A

56131705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128357580-C-G

56131705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128357580-C-T

56131714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128357571-T-C

56131714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128357571-T-G

56131897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128357402-T-A

56131897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128357402-T-C

56131929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128357373-G-A

56131929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128357373-G-T

56131936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128357366-A-G

56132210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 128356896-T-C

56132288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128356818-C-T

56132523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: missense variant
orthologous variants: 128356585-C-T

56132635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128356308-C-G

56132635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128356308-C-T

56132672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128356268-C-T

56132863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128356106-G-A

56132872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128356097-G-C

56133314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128355844-G-A

56133314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128355844-G-T

http://identifiers.org/hco/12/GRCh38#56133320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128355838-C-A

56133331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128355828-G-A

56133339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128355820-G-T

56133400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128355723-C-G

http://identifiers.org/hco/12/GRCh38#56133403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128355720-C-A

56133404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128355719-C-T

56133494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128355635-C-G

56133603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: missense variant
orthologous variants: 128355537-G-A

http://identifiers.org/hco/12/GRCh38#56133763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128355405-A-C

56133886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128355274-G-A

56133902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128355257-T-C

56134396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: missense variant
orthologous variants: 128354827-C-G

56134396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: stop gained
orthologous variants: 128354827-C-T

56134485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128354743-T-C

56136637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128353729-T-G

56136638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128353728-G-C

56136638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128353728-G-T

56136642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128353724-T-C

56136642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128353724-T-G

56136653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128353717-A-G

56136653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128353717-A-T

56136731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128353644-C-T

56136802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: missense variant
orthologous variants: 128353573-T-A

56136991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128353407-T-A

56137021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128353390-A-G

56137038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: 128353373-G-T

http://identifiers.org/hco/12/GRCh38#56137136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128353332-C-A

56137415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128353073-C-G

56137745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128352744-A-G

56137963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128352490-C-T

56138017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128352454-C-T

56138078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128352396-A-G

56138335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128352179-G-C

http://identifiers.org/hco/12/GRCh38#56138513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128351998-C-A

56138513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128351998-C-T

56138556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128351944-G-A

56138556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128351944-G-T

56138685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128351874-G-A

56138685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128351874-G-T

56138701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128351859-A-T

56138740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128351830-T-A

56138784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128351787-A-G

56138792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128351779-A-G

56138881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128351690-G-A

56138892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128351675-A-G

56138904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128351663-T-A

56142179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128348399-T-C

56142276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128348340-G-A

56142414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128348205-G-A

56142641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128348016-T-A

56142683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128347974-A-G

56142683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128347974-A-T

56142743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128347914-G-A

56143010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 128347660-G-A

56143179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128347497-G-A

56143223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 128347443-C-T

56143406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128347293-G-A

56143454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128347229-G-T

56143461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128347222-G-A

56143556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128346920-T-G

56143610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128346866-T-C

56143693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128346779-A-G

http://identifiers.org/hco/12/GRCh38#56143804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128346553-A-C

56143804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128346553-A-G

56143889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128346458-T-C

56143909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128346444-T-G

56143921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128346436-C-T

56144012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128346352-G-A

56144104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128346263-T-C

56144104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128346263-T-G

http://identifiers.org/hco/12/GRCh38#56144342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#128345913-C-A

56144342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128345913-C-T

56144359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128345898-T-C

56144446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128345810-T-C

56144646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29534
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128345599-A-G