118981597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5 prime UTR variant
orthologous variants: 116729818-G-T

118981643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5 prime UTR variant
orthologous variants: 116729773-A-G

118981643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5 prime UTR variant
orthologous variants: 116729773-A-T

118981681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116729741-G-A

118981681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116729741-G-T

http://identifiers.org/hco/12/GRCh38#118981691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116729731-C-A

118981691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116729731-C-G

118981691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116729731-C-T

http://identifiers.org/hco/12/GRCh38#118981705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116729714-C-A

118981705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116729714-C-T

http://identifiers.org/hco/12/GRCh38#118981716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116729703-C-A

118981716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116729703-C-G

118981716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116729703-C-T

118981720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5 prime UTR variant
orthologous variants: 116729699-G-A

118981720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5 prime UTR variant
orthologous variants: 116729699-G-T

http://identifiers.org/hco/12/GRCh38#118981816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116729589-C-A

118981816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116729589-C-G

118981816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116729589-C-T

http://identifiers.org/hco/12/GRCh38#118981869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116729536-C-A

118981869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5 prime UTR variant
orthologous variants: 116729536-C-G

118981869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5 prime UTR variant
orthologous variants: 116729536-C-T

118981872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5 prime UTR variant
orthologous variants: 116729533-T-C

118981872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 5 prime UTR variant
orthologous variants: 116729533-T-G

118982047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116729357-A-G

118982116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116729283-T-A

118982116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116729283-T-C

118982120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116729278-T-C

118982278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116729121-G-A

118982682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116728752-T-A

118982682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116728752-T-G

118982837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116728624-T-C

118983010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116728465-G-A

118983028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116728449-C-G

http://identifiers.org/hco/12/GRCh38#118983139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116728341-C-A

118983158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116728322-T-A

118983180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116728296-T-C

118983256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116728224-G-A

118983293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116728182-G-A

118983360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116728118-T-G

118983367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116728111-G-A

118983367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116728111-G-C

http://identifiers.org/hco/12/GRCh38#118983387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116728099-C-A

118983387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116728099-C-T

118983503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116727973-A-G

118983558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116727921-A-G

118983603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116727877-C-G

118983718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116727772-G-A

118984013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116727466-T-C

118984461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116727065-G-A

http://identifiers.org/hco/12/GRCh38#118984685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116726854-A-C

http://identifiers.org/hco/12/GRCh38#118984716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116726813-C-A

118984726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116726803-G-A

118984825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116726708-T-G

118984828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116726705-T-C

118984951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116726586-A-G

118985649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116725508-G-A

118985740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116725431-G-T

118986149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116725017-C-T

118986291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116724877-C-T

118986391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116724777-G-T

118986433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116724764-C-G

118986944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116724323-G-A

118986976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116724293-C-T

118986985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116724284-A-G

118987471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116723732-C-G

118987563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116723660-C-T

118987600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116723624-C-T

118987824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116723385-C-T

118987851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116723360-C-G

118988090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116723334-G-A

118988090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116723334-G-C

118988369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116723051-T-C

118988784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116722612-T-A

118988855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116722568-G-C

118988974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116722451-T-A

118989003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116722422-G-A

118989093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116722359-T-A

118989164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116722291-T-C

118989537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116721938-C-T

http://identifiers.org/hco/12/GRCh38#118989561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116721914-C-A

118989787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116721682-G-T

118989830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116721650-T-C

http://identifiers.org/hco/12/GRCh38#118989854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116721624-C-A

118989854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116721624-C-T

http://identifiers.org/hco/12/GRCh38#118989867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116721611-C-A

118989881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116721597-A-G

118989931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116721547-A-G

118990365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116721744-C-G

118992356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116721143-G-T

118992628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116720863-G-T

118992701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116720789-G-A

118993015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116720504-A-G

118993017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116720502-A-G

118994309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116720189-T-G

118995209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116719416-T-A

118995289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116719345-T-C

118995991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116718740-T-C

118996056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116718674-T-C

118996100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116718629-A-G

118996100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116718629-A-T

118996482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116718077-A-T

118997127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116717393-C-T

118997490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116717044-A-G

118997613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116716931-C-G

118997781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116716782-C-T

118997792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116716773-T-A

118997838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116716733-A-T

118997957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116716641-C-T

http://identifiers.org/hco/12/GRCh38#118998114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116716494-A-C

118998187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116716422-T-C

http://identifiers.org/hco/12/GRCh38#118998301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116716348-C-A

118998353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116716295-G-A

118998407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116716204-A-G

118998560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116716050-C-T

118998713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116715890-T-C

http://identifiers.org/hco/12/GRCh38#118999023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116715571-C-A

118999023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116715571-C-T

118999102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116715504-G-A

118999222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116715383-G-C

118999398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116715226-G-A

118999416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116715208-C-T

118999523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116715097-A-G

118999671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116714957-A-G

119000002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116714712-T-C

119000061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116714667-A-T

119000173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116714561-T-A

119000173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116714561-T-G

119000358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116714353-T-C

119000501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116714184-C-T

http://identifiers.org/hco/12/GRCh38#119000514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116714171-C-A

119000554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116714138-G-C

119000591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116714102-G-A

119000675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116714019-T-A

http://identifiers.org/hco/12/GRCh38#119000688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116714006-C-A

119000705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116713990-G-A

119000749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116713946-A-G

119005843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116710475-T-C

119005846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116710472-A-G

119006107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116710201-T-A

119006107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116710201-T-C

119006213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116710098-G-C

119006261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116710053-C-T

119006378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116709898-G-A

119006391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116709885-T-C

119006664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116709709-C-T

119006836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116709551-A-G

119007013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116709388-G-A

119007166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116709215-G-A

http://identifiers.org/hco/12/GRCh38#119007293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116709094-A-C

119007353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116709056-A-G

119007888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116708422-T-A

119008060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116708295-C-G

119008060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116708295-C-T

119008062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116708293-G-T

119009016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116707721-G-A

119009045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116707672-G-A

119009214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116707522-T-C

119009218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116707518-C-T

119009313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116707349-C-T

119009330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116707333-G-A

http://identifiers.org/hco/12/GRCh38#119009404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116707265-C-A

119009404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116707265-C-T

119009884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116706797-T-C

119010590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116705961-A-G

119011307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116705041-T-G

119011493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116704858-G-A

119011785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116704614-T-G

119011849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116704542-A-G

119011989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116704114-A-G

119012092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116704023-T-A

119012092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116704023-T-C

http://identifiers.org/hco/12/GRCh38#119012441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116703722-C-A

119012659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116703512-G-A

119014120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116702376-G-A

119014154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116702340-C-T

119014285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116702202-G-T

119014309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116702178-G-T

119014317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116702170-A-G

119014358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116702129-A-T

119014360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116702127-A-G

119014363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116702114-G-A

http://identifiers.org/hco/12/GRCh38#119014484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116701987-C-A

119014486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116701985-T-C

119014563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116701913-C-G

119014701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116701770-G-T

http://identifiers.org/hco/12/GRCh38#119014852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116701625-C-A

119014986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116701481-A-G

119015012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116701454-G-T

119015248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116701171-A-G

119015276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116701143-G-C

119015430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116700993-C-T

119015537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116700920-C-G

http://identifiers.org/hco/12/GRCh38#119015546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116700911-A-C

119015961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116700726-T-C

119016490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116699648-G-A

119016495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116699643-C-T

119016598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116699542-G-T

119016904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116699267-T-A

119016915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116699256-C-T

119018993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116697875-A-G

119018995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116697873-A-G

119019022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116697855-T-G

119019023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116697854-C-T

119019076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116697809-C-T

http://identifiers.org/hco/12/GRCh38#119019139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116697745-C-A

119019165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116697719-A-T

119019308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116697570-T-C

119019341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116697538-C-T

119019389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116697472-C-T

119020466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116695333-G-T

119020480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116695319-C-T

http://identifiers.org/hco/12/GRCh38#119020551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116695249-A-C

119020639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116695158-G-T

http://identifiers.org/hco/12/GRCh38#119020696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116695102-A-C

119020799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116694999-G-A

119020799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116694999-G-C

119020913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, undefined
orthologous variants: 116694895-A-G

119020979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, undefined
orthologous variants: 116694829-G-C

119021350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116693866-G-A

119021642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116693580-C-T

119022428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116693369-T-A

119022519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116693297-C-T

119022523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116693293-C-T

119022644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116693173-G-A

http://identifiers.org/hco/12/GRCh38#119022935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116692891-C-A

119023078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116692763-T-A

119023078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116692763-T-G

119023307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116692545-T-A

119023390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116692473-A-G

119023722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116692147-G-C

119023768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116692103-A-G

119024169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116691724-C-T

119024240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116691653-A-G

119024325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116691573-T-G

119024339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116691566-G-A

119024690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116691313-G-C

119024707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116691296-G-A

119024765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116691236-C-T

119024900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116691116-T-C

119027269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116687645-T-G

119029129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116685437-G-A

119029167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116685398-A-G

119029176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116685389-T-G

119029248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116685320-C-G

119029300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116685267-T-C

119029333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116685234-G-T

119029696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116684638-T-C

119029807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116684530-T-C

119029865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116684473-A-G

http://identifiers.org/hco/12/GRCh38#119030113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116684226-C-A

119030113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116684226-C-T

119030205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116684132-G-A

119030251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116684086-C-T

119030486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116683895-C-T

119030548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116683772-T-C

119030728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116683481-T-C

119030825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116683393-G-A

119030825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116683393-G-T

119030952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116683269-A-G

119035859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116678142-A-G

http://identifiers.org/hco/12/GRCh38#119036286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116677743-A-C

119036510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677526-C-G

119036603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677452-T-A

119036603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677452-T-C

119036731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677332-G-A

119036733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677330-G-A

119036733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677330-G-C

119036733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677330-G-T

119036740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677323-G-A

119036757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677305-A-G

119036782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116677280-T-C

119036797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116677264-T-C

http://identifiers.org/hco/12/GRCh38#119036841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116677224-C-A

119036845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116677220-T-C

119036866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116677193-A-G

119036947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116676980-T-A

119037026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676817-G-T

http://identifiers.org/hco/12/GRCh38#119037076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116676759-A-C

119037076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116676759-A-G

119037168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676672-C-G

119037182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676658-T-C

119037182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676658-T-G

119037225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676540-G-A

119037276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676488-T-C

http://identifiers.org/hco/12/GRCh38#119037292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116676472-C-A

119037488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676273-T-A

119037493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116676268-T-C

119038098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675638-G-A

119038336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675521-C-G

119038336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675521-C-T

119038598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116675455-G-T

119039038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674996-G-A

119039050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674984-A-G

119039081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674934-A-T

119039236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674801-C-T

119039278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674761-A-G

119039374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674661-A-G

119039529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674537-A-G

119039603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674466-C-T

119039746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674347-C-G

119039763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674331-T-A

119039802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674292-T-C

119039850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674262-G-A

http://identifiers.org/hco/12/GRCh38#119039971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116674141-A-C

119039971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674141-A-G

119039991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674126-A-G

119039998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674119-G-A

119040055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674071-A-G

119040129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116674001-G-A

http://identifiers.org/hco/12/GRCh38#119040138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116673992-C-A

119041489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116671717-G-A

119041606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116671607-T-C

119041677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116671542-G-A

http://identifiers.org/hco/12/GRCh38#119041846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116671440-A-C

119042015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116671320-C-T

119042023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116671319-C-T

119042270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116671085-C-T

119042310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116671048-G-A

119042353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116670992-A-G

http://identifiers.org/hco/12/GRCh38#119042545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116670800-A-C

119042735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116670613-G-A

119043614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

119043709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

119043735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/12/GRCh38#119043747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

119044319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116670131-T-C

119044352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116670099-G-T

119044476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116669979-G-A

119044554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116669905-G-A

119044601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116669869-C-T

119044866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116668836-A-G

119044886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116668812-C-G

119044923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116668775-C-T

119045061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116668644-C-T

119045121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116668585-T-C

119045176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116668539-T-C

119045298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116668416-C-T

119045329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116668388-T-C

119045338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116668379-C-T

119046267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116668228-G-A

119046526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116667988-A-G

119046630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116667872-A-G

119049833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116667005-A-G

http://identifiers.org/hco/12/GRCh38#119049936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116666960-A-C

119050081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116666831-A-G

119050347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116666594-T-G

http://identifiers.org/hco/12/GRCh38#119050365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116666564-A-C

119050365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116666564-A-T

http://identifiers.org/hco/12/GRCh38#119050532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116666386-A-C

119050537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116666381-G-A

119050552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116666366-G-A

119050552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116666366-G-C

119050728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116666203-A-G

http://identifiers.org/hco/12/GRCh38#119050788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116666120-C-A

119050876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116665938-T-C

119051013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116665805-C-T

119051432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116665382-C-T

119051754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116665007-C-T

119051905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116664850-A-G

119051949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116664803-G-A

119052060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116664691-T-C

119052090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116664661-G-C

119052335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116664431-G-A

119052353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116664413-G-A

119052363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116664409-A-G

http://identifiers.org/hco/12/GRCh38#119052418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116664355-A-C

119052442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116664293-T-C

http://identifiers.org/hco/12/GRCh38#119053066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116663884-A-C

119053220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116663746-A-G

119053389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116663578-G-A

119053389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116663578-G-C

119053441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116663545-T-C

119053543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116663460-C-T

119053705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116663305-T-A

119054617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116662668-A-G

119055003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116662344-G-C

119055038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116662311-C-T

119055115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116662253-G-A

119055358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116662050-G-A

119055365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116662043-T-A

119055426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116661980-C-T

119055545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116661863-C-T

119055665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116661758-G-A

119055665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116661758-G-C

119055697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116661726-G-A

119055836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116661611-T-C

http://identifiers.org/hco/12/GRCh38#119055927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116661534-C-A

119056227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116661236-T-C

119056509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116660914-C-G

119056662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116660776-C-G

119056670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116660768-T-G

http://identifiers.org/hco/12/GRCh38#119056678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116660760-A-C

119056988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116660492-C-T

119057004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116660463-G-A

119057004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116660463-G-T

119057025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116660442-A-G

119057085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116660387-A-G

119057103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116660360-C-T

119058475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116659543-T-C

119058878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116659239-T-C

119058883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116659234-C-T

http://identifiers.org/hco/12/GRCh38#119059165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116658961-C-A

119059192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116658934-C-T

http://identifiers.org/hco/12/GRCh38#119059299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116658826-C-A

119059299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116658826-C-T

119059667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116658444-G-T

119059691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116658420-T-C

119059740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116658367-T-G

http://identifiers.org/hco/12/GRCh38#119059850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116658279-C-A

119059863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116658266-C-G

119059898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116658234-G-A

http://identifiers.org/hco/12/GRCh38#119059902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116658230-C-A

119060223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116657915-A-G

119060246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116657876-T-C

119060338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116657787-G-A

119060343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116657782-T-C

119060397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116657725-T-C

119060481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116657652-A-G

119060489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116657644-A-G

119060580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116657596-T-G

119060581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116657595-T-A

119060595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116657582-T-C

119060647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116657530-A-T

119060877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116657313-G-A

119061262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116656441-G-C

119061361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116656348-G-C

119061485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116656274-G-A

119061542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116656207-G-A

http://identifiers.org/hco/12/GRCh38#119063632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116654641-C-A

119063992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116654521-A-G

119064899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116653596-T-C

119065042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116653453-T-G

119065279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116653232-C-T

119065436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116653064-T-G

119065437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116653063-T-C

119065781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116652784-G-A

119065790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116652775-T-C

119065799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116652766-G-T

119065814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116652751-T-C

119065874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116652675-T-G

119066189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116652289-T-C

119066241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116652245-T-C

119067061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116651440-G-T

119067229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116651275-T-C

119067995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116650408-T-C

http://identifiers.org/hco/12/GRCh38#119068017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116650386-A-C

119068041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116650377-A-G

119068386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116650034-A-G

119068587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116649904-T-C

119068587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116649904-T-G

http://identifiers.org/hco/12/GRCh38#119069210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116649286-A-C

119069210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116649286-A-T

119069236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116649266-C-T

119069650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116648448-G-A

119069686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116648417-G-A

119069686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116648417-G-C

119069740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116648362-C-T

119069755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116648347-G-T

119069820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116648291-C-T

119069822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116648289-T-C

http://identifiers.org/hco/12/GRCh38#119069826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116648285-C-A

119069835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116648276-G-A

119069960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116648151-G-A

119070098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116647997-G-C

http://identifiers.org/hco/12/GRCh38#119070182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116647912-C-A

119070218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116647876-A-G

http://identifiers.org/hco/12/GRCh38#119070220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116647874-A-C

119070431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116647699-A-G

119070487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116647649-G-A

119070516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116647620-C-G

119070956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116647246-G-A

119071162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116647035-T-G

119071248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116646838-T-C

119071505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116646449-T-G

119071531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116646418-A-G

119071603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116646351-T-A

119071844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116646083-A-G

119071969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116645977-C-T

119071992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116645849-C-T

http://identifiers.org/hco/12/GRCh38#119072042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116645805-C-A

119072178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116645676-A-T

119072226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116645629-A-G

119072254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116645600-C-T

119072481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116645382-T-C

119072677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116645177-T-A

119072677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116645177-T-C

119072767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116645098-T-A

119072777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116645085-C-G

119072808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116645055-T-C

119072960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644922-T-C

119072987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644896-G-T

119073004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644879-A-G

119073043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644840-G-T

119073085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644786-A-G

119073138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644740-A-G

119073143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644735-A-G

119073145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644733-T-C

119073178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644700-G-A

119073190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644688-G-A

119073978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644563-A-G

119074076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644466-A-G

119074105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644436-C-T

119074196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644346-G-C

119074316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116644213-A-G

119074593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116643894-A-G

119074780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116643650-A-G

119075012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116643443-G-A

119075035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116643420-G-C

119075035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116643420-G-T

119075093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116643361-T-C

119075097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116643357-T-G

http://identifiers.org/hco/12/GRCh38#119075304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116643150-C-A

119075304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116643150-C-T

119076088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116642933-A-G

119076089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116642932-T-G

119076093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116642928-G-A

http://identifiers.org/hco/12/GRCh38#119076112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116642910-A-C

http://identifiers.org/hco/12/GRCh38#119076314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116642761-C-A

119076345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116642733-T-G

119076435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116642628-A-G

119076577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116642494-T-C

119076641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116642445-T-C

119076641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116642445-T-G

119076696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116642391-G-A

119076795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116642293-C-T

119076850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116642238-T-A

119076865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116642223-G-A

119076870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116642216-G-T

119076916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116642151-G-A

119077329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116641711-G-T

119077357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116641691-G-A

119078007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116641000-G-A

119078054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116640959-G-T

119078104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116640909-G-A

119078428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116640650-T-C

119079299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116640071-G-A

119079540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116639831-G-C

119079716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116639655-G-A

119079840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116639532-G-A

119080400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116639024-A-G

119080484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116638944-A-G

119080500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116638933-G-A

http://identifiers.org/hco/12/GRCh38#119080528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116638915-A-C

http://identifiers.org/hco/12/GRCh38#119080559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116638885-C-A

119080577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116638867-C-T

119080712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116638767-T-A

119080712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116638767-T-C

119080712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116638767-T-G

119080760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116638722-C-G

http://identifiers.org/hco/12/GRCh38#119080806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116638674-C-A

119081128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116638580-C-G

119081521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116638198-G-A

119081524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116638195-C-G

119081688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116638037-G-A

119081751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116637962-G-A

119081802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116637890-T-C

119082002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116637720-A-G

119082109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116637622-T-C

http://identifiers.org/hco/12/GRCh38#119082143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116637587-C-A

119082143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116637587-C-T

http://identifiers.org/hco/12/GRCh38#119082302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116637458-C-A

119082302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116637458-C-T

119082385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116637370-T-C

http://identifiers.org/hco/12/GRCh38#119082651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116637093-C-A

119082651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116637093-C-T

http://identifiers.org/hco/12/GRCh38#119082752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116636808-C-A

119082752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116636808-C-T

119082824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116636720-A-G

119082999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116636482-G-T

119083119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116636360-G-A

119083119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116636360-G-T

119083139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116636337-T-C

119083756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116635848-C-T

119085274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116635776-T-C

119085430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116635632-C-T

119085477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116635598-C-T

119085483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116635592-T-G

119085513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116635563-T-A

119085597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116635489-A-G

119085624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116635458-C-T

119085723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116635369-G-C

119085801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116635306-G-A

119085842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116635267-G-A

119086348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116635001-G-A

119086580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116634780-T-C

http://identifiers.org/hco/12/GRCh38#119086594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116634766-A-C

119086594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116634766-A-G

119086662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116634711-G-C

119086852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116634538-C-T

119087041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116634346-G-A

119087167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116634245-G-A

119087230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116634196-G-A

119087242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116634184-G-C

119087260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116634166-G-A

119087413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116634023-G-A

119087663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633762-A-G

119087731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633680-T-C

119087796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633632-C-T

119087797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633631-C-T

119087813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633615-G-A

119087903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633526-G-A

119087903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633526-G-C

119087903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633526-G-T

119087941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633510-C-T

119087998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633455-G-T

119088115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633390-G-A

119088310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633236-T-A

119088362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633184-C-T

119088384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633163-C-T

http://identifiers.org/hco/12/GRCh38#119088436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116633111-C-A

119088436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633111-C-T

119088481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633069-G-A

119088526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116633020-G-A

119088596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116632952-A-G

119088627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116632942-G-C

http://identifiers.org/hco/12/GRCh38#119088698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116632904-C-A

119088698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116632904-C-T

119088729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116632872-G-A

119088743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116632858-G-A

119088834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116632766-C-T

119088867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116632733-C-T

119088897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116632703-C-T

119088915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116632685-G-A

http://identifiers.org/hco/12/GRCh38#119088921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116632679-C-A

119089226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116632411-G-A

http://identifiers.org/hco/12/GRCh38#119089229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116632399-C-A

119089229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116632399-C-T

119089244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116632384-T-C

119089282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116632342-T-C

119089399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116632224-A-G

119089436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116632188-T-C

119089720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116631939-T-C

119089722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116631937-T-C

119090770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116630309-C-T

119090785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116630296-G-C

119090785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116630296-G-T

119090891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116630219-C-G

119091026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116630074-T-C

119091368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116629384-C-T

119091391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116629362-G-T

119091404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116629349-A-G

119091431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116629323-C-T

119091734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116629096-A-G

http://identifiers.org/hco/12/GRCh38#119091861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116628982-C-A

119091863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116628980-C-T

119092006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116628848-C-G

119092340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116628557-A-G

119093067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116626914-A-T

119093101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116626873-C-T

119093389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116626532-T-A

119093700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116626013-T-C

119093847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116625919-T-C

119093961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116625791-T-C

119094008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116625741-G-C

119094011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116625738-T-C

119094083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116625665-G-A

119094135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116625608-C-T

http://identifiers.org/hco/12/GRCh38#119094314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116625320-C-A

119094314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116625320-C-T

http://identifiers.org/hco/12/GRCh38#119094630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116625062-C-A

119094638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116625054-A-G

119094646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116625046-C-T

119094667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116625026-A-G

119094887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116624830-T-C

119095280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116624471-T-C

119095439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116624328-G-A

119096488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116623826-T-G

119096634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116623654-G-A

119096992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116623234-T-G

119097049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116623163-C-T

119097052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116623160-C-T

119097334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116622881-C-T

119097632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116621489-T-C

119102147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116620670-G-A

119102166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116620656-G-T

119102307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116620522-C-T

119102362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 116620467-G-T

119102421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116620393-A-G

119102531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116620301-A-G

http://identifiers.org/hco/12/GRCh38#119102550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116620282-C-A

http://identifiers.org/hco/12/GRCh38#119112099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116617140-C-A

http://identifiers.org/hco/12/GRCh38#119113863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116615589-A-C

119113901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116615553-C-G

http://identifiers.org/hco/12/GRCh38#119114024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116615430-C-A

119114024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116615430-C-T

http://identifiers.org/hco/12/GRCh38#119114132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116615325-C-A

119114132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116615325-C-G

119114132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116615325-C-T

http://identifiers.org/hco/12/GRCh38#119114134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116615323-C-A

http://identifiers.org/hco/12/GRCh38#119114138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116615319-C-A

119114138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116615319-C-T

http://identifiers.org/hco/12/GRCh38#119114217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116615250-C-A

119114241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116615239-A-G

119114297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116615183-T-A

119114378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116615103-G-A

119114378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116615103-G-C

119114683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116614838-G-T

http://identifiers.org/hco/12/GRCh38#119115006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116614652-A-C

119115028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116614630-A-G

119115127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116614537-C-T

119115322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116614391-T-C

http://identifiers.org/hco/12/GRCh38#119115437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116614303-C-A

119115485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116614255-G-A

119115538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116614202-G-T

119116426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116613704-C-G

119116700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116613426-C-T

119116827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116613369-T-C

119116833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116613363-T-C

119117074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116613170-T-A

http://identifiers.org/hco/12/GRCh38#119117116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116613124-A-C

119117144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116613103-G-A

119117172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116613082-G-A

119117615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116612700-C-T

119117616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116612699-G-A

119117618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116612697-G-A

119117618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116612697-G-C

119117623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116612692-T-G

http://identifiers.org/hco/12/GRCh38#119117984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116612564-C-A

119118473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116612203-G-A

119118663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116612047-G-A

119118826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116611900-A-G

http://identifiers.org/hco/12/GRCh38#119118857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116611877-A-C

119118860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116611874-G-A

119118870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116611862-G-A

119119024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116611714-G-A

119119127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116611631-T-G

119119231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116611495-A-T

119119756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610997-T-G

http://identifiers.org/hco/12/GRCh38#119119868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116610853-C-A

119120011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610729-C-T

119120047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610694-C-T

http://identifiers.org/hco/12/GRCh38#119120081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116610678-A-C

119120115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610657-T-A

119120115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610657-T-C

119120115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610657-T-G

http://identifiers.org/hco/12/GRCh38#119120117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116610655-A-C

119120117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610655-A-G

http://identifiers.org/hco/12/GRCh38#119120126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116610646-C-A

119120126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610646-C-T

http://identifiers.org/hco/12/GRCh38#119120181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116610614-C-A

119120181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610614-C-G

119120181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610614-C-T

119120182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610613-T-A

119120182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610613-T-C

http://identifiers.org/hco/12/GRCh38#119120307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116610531-A-C

119120307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610531-A-T

119120318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610520-T-G

119120323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610517-A-G

119120407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610437-T-C

http://identifiers.org/hco/12/GRCh38#119120418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116610426-A-C

119120418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610426-A-G

119120420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610424-G-T

119120603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116610334-C-T

119121360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116609934-T-A

119121754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116609587-T-C

119121763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116609580-T-C

http://identifiers.org/hco/12/GRCh38#119121976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116609424-C-A

119121983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116609417-T-A

119121983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116609417-T-C

119121999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116609405-G-A

119121999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116609405-G-T

119122161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116609255-A-G

119122187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116609230-C-T

119122198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116609219-G-T

119122451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116609041-G-T

119122459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116609036-G-T

119122659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116608809-G-A

119122829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116608605-G-A

119123079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116608357-C-T

119123184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116608254-G-C

119123241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116608197-G-A

119123325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116608097-G-A

119123370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116607979-T-C

http://identifiers.org/hco/12/GRCh38#119123416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116607926-C-A

119123555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116607782-C-T

119123942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116607508-G-A

119124087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116607354-G-A

119124087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116607354-G-T

http://identifiers.org/hco/12/GRCh38#119124132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116607314-A-C

119124132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116607314-A-G

http://identifiers.org/hco/12/GRCh38#119124161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116607255-A-C

119124161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116607255-A-G

119124229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116607196-T-A

http://identifiers.org/hco/12/GRCh38#119124256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116607171-C-A

119124256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116607171-C-T

http://identifiers.org/hco/12/GRCh38#119124305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116607127-A-C

http://identifiers.org/hco/12/GRCh38#119124312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116607120-C-A

119124331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116607097-G-C

119124337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116607092-G-A

119124337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116607092-G-T

119124363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116607066-T-A

119124424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116607000-A-G

119124442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116606982-T-C

119124722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116606619-C-G

119124925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116606409-T-C

http://identifiers.org/hco/12/GRCh38#119125315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116605982-C-A

119125315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116605982-C-G

119125315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116605982-C-T

http://identifiers.org/hco/12/GRCh38#119125359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116605939-C-A

119125359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116605939-C-T

119125364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116605934-C-T

119125448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116605856-T-A

119125512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116605792-G-A

119125512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116605792-G-T

119130649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116605679-A-G

119130661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116605667-C-G

119130683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116605640-G-A

119130918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116605407-G-A

119130918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116605407-G-C

119130918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116605407-G-T

119130920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116605405-A-G

119130920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116605405-A-T

http://identifiers.org/hco/12/GRCh38#119130937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116605388-C-A

119131235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116605124-G-A

119131264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116605095-T-C

http://identifiers.org/hco/12/GRCh38#119131285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116605074-A-C

119131372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116605020-C-T

119132039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116604381-G-C

119132174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116604256-C-T

119132231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116604143-A-G

119132359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 116604032-A-G

119132377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116604014-A-G

119132438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116603953-G-A

119132438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116603953-G-T

119132487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116603904-T-C

119132580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116603813-C-T

119132584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116603809-G-A

119132597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116603796-C-T

119132687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116603685-C-T

http://identifiers.org/hco/12/GRCh38#119132795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116603553-A-C

119132928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116603432-T-A

119132928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116603432-T-C

119132938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116603423-T-C

119132981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116603410-G-A

119133143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116603289-T-C

119133188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116603245-G-A

http://identifiers.org/hco/12/GRCh38#119133278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116603155-C-A

119133368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116603146-T-C

119133410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116603105-T-C

119133495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116603012-C-T

119133526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116602980-C-T

119133782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116602751-C-G

119134132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116602487-T-C

119134132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116602487-T-G

http://identifiers.org/hco/12/GRCh38#119134512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116602297-C-A

119134716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116602102-G-A

119134903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116601932-T-C

119135032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116601806-A-G

119135106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116601731-G-A

119135251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116601652-G-A

119135366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116601544-C-G

119135403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116601510-T-C

119135666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116601306-T-C

119136081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116600552-T-A

119136081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116600552-T-C

119136097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116600536-C-G

119136195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116600466-G-A

119136233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116600428-A-G

119136236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116600425-T-C

119136256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116600405-G-A

119136291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116600402-A-G

119136445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116600332-G-A

119136587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116600229-A-G

119136780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116600014-A-G

119136846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116599946-A-G

119136909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116599886-C-T

119136941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116599848-A-G

119137079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116599735-T-A

http://identifiers.org/hco/12/GRCh38#119137390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116599427-C-A

119137391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116599426-C-T

119137573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116599244-G-T

119137648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116599145-T-G

119137874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116598706-G-C

http://identifiers.org/hco/12/GRCh38#119137914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116598667-C-A

119138028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116598561-A-G

119138158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116598487-G-A

119138158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116598487-G-C

119138459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116598199-T-C

119138572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116598086-T-C

119138655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116598013-A-G

http://identifiers.org/hco/12/GRCh38#119138704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116597966-A-C

119138719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116597951-T-C

119138812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116597852-T-C

http://identifiers.org/hco/12/GRCh38#119138893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116597697-A-C

119139279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116597326-C-T

119139321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116597305-C-T

119139353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116597260-C-T

http://identifiers.org/hco/12/GRCh38#119139545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116597063-C-A

119139796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116596853-G-T

119139818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116596834-C-G

119141650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116595392-G-A

119141650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116595392-G-T

119142054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116595055-A-G

119142145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116594953-G-T

119142183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116594915-T-C

119142294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116594816-C-T

119142382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116594733-C-T

119142769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116594399-T-C

119142959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116594256-T-C

119143001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116594085-C-G

119143001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116594085-C-T

119143318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116593784-A-G

119143495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116593604-T-A

119143563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116593546-T-C

http://identifiers.org/hco/12/GRCh38#119143658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116593464-C-A

119143658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116593464-C-T

http://identifiers.org/hco/12/GRCh38#119143857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116593309-C-A

119143934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116593238-C-T

119143954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116593218-G-A

http://identifiers.org/hco/12/GRCh38#119143993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116593180-A-C

http://identifiers.org/hco/12/GRCh38#119144090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116593101-A-C

119144163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116593034-C-T

119144226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116592984-C-G

119144226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116592984-C-T

119144390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116592880-G-A

119144390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116592880-G-T

119144790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116592465-A-G

119144870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116592326-C-G

119145100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116592079-T-C

119145235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116591902-T-A

119145235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116591902-T-C

119145335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116591816-A-G

http://identifiers.org/hco/12/GRCh38#119145544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116591607-C-A

119145650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116591501-G-T

http://identifiers.org/hco/12/GRCh38#119145660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116591491-C-A

119145660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116591491-C-T

119145709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116591451-G-A

119145709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116591451-G-T

119145799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116591365-G-C

119145799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116591365-G-T

119145817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116591354-G-A

119145817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116591354-G-T

119148069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116589792-G-A

119148098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116589762-A-G

119148465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116589657-T-C

119148471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116589651-T-C

119148568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116589555-C-T

119148642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116589474-A-G

119148676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116589438-C-G

119148874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116589251-T-A

http://identifiers.org/hco/12/GRCh38#119148875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116589250-A-C

119148875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116589250-A-T

119148958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116589165-G-A

119149569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116588814-C-G

119149581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116588799-G-A

119149916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116588500-C-T

119149917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116588499-C-G

119150055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116588349-A-G

119150504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116588210-C-T

119150759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116587947-C-T

119150766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116587940-G-A

http://identifiers.org/hco/12/GRCh38#119150984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116587715-A-C

119150989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116587712-G-T

119151255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116587446-T-C

http://identifiers.org/hco/12/GRCh38#119151297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116587366-C-A

119151665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116587010-T-C

119151739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116586908-C-G

119151739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116586908-C-T

119151950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116586650-C-G

119151971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116586619-G-A

119152043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116586542-C-T

119152103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116586481-C-T

119152152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116586434-T-G

119153390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116585563-C-T

119153454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116585517-G-C

119153454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116585517-G-T

http://identifiers.org/hco/12/GRCh38#119153476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116585492-C-A

119153476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116585492-C-T

119153484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116585485-G-A

119153544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: missense variant
orthologous variants: 116585416-A-G

119153544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: missense variant
orthologous variants: 116585416-A-T

119153585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: missense variant
orthologous variants: 116585375-A-G

119153652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116585308-A-G

119153661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116585300-G-A

119153661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116585300-G-C

119153661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116585300-G-T

http://identifiers.org/hco/12/GRCh38#119153689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116585278-C-A

119153689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116585278-C-T

119153703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116585264-T-C

119153710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116585257-C-T

http://identifiers.org/hco/12/GRCh38#119153711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116585256-C-A

119153711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116585256-C-G

http://identifiers.org/hco/12/GRCh38#119153734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116585233-C-A

http://identifiers.org/hco/12/GRCh38#119153747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116585216-C-A

119153747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116585216-C-T

119153957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116584973-G-A

119153957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116584973-G-T

119154087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116584828-C-T

119154145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116584783-A-G

http://identifiers.org/hco/12/GRCh38#119154187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116584758-C-A

119154187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116584758-C-G

119154187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116584758-C-T

http://identifiers.org/hco/12/GRCh38#119154205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116584740-C-A

119154205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116584740-C-T

http://identifiers.org/hco/12/GRCh38#119154235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116584689-C-A

119154235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 116584689-C-G

119154235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 116584689-C-T

http://identifiers.org/hco/12/GRCh38#119154247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116584677-C-A

119154247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: missense variant
orthologous variants: 116584677-C-T

119154338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: missense variant
orthologous variants: 116584592-G-A

119154338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: missense variant
orthologous variants: 116584592-G-T

119154489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116584436-A-G

119154491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116584434-G-C

119154495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116584430-G-A

119154495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116584430-G-C

119154495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116584430-G-T

http://identifiers.org/hco/12/GRCh38#119154525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116584397-A-C

119154526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116584396-T-C

http://identifiers.org/hco/12/GRCh38#119154632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116584306-A-C

119154781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116584189-G-A

119155184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116583843-A-T

http://identifiers.org/hco/12/GRCh38#119155241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116583777-C-A

119155291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116583736-T-C

119155293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116583734-G-C

119155339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116583669-A-G

119156334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116583156-T-C

119156344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116583151-T-A

119156368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116583114-G-A

119156368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116583114-G-T

119156371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116583111-A-T

119156409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116583006-T-C

119156432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116582984-G-A

http://identifiers.org/hco/12/GRCh38#119156476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116582950-C-A

119156476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: intron variant
orthologous variants: 116582950-C-T

119156577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: missense variant
orthologous variants: 116582849-A-G

119156593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: missense_variant, undefined
orthologous variants: 116582815-C-G

119156593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: missense_variant, undefined
orthologous variants: 116582815-C-T

http://identifiers.org/hco/12/GRCh38#119156679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#116582714-C-A

119156679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: missense_variant, undefined
orthologous variants: 116582714-C-G

119156679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: missense_variant, undefined
orthologous variants: 116582714-C-T

119156797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: undefined
orthologous variants: 116582626-A-G

119156801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582614-G-T

http://identifiers.org/hco/12/GRCh38#119156804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116582611-C-A

119156804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582611-C-T

119156807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582608-G-A

119156807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582608-G-T

119156833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582579-C-G

119156833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582579-C-T

119156887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582521-A-G

119156891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582517-A-G

http://identifiers.org/hco/12/GRCh38#119156900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116582508-A-C

http://identifiers.org/hco/12/GRCh38#119156971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116582440-C-A

119156971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582440-C-G

119157010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582402-T-C

http://identifiers.org/hco/12/GRCh38#119157095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116582367-C-A

119157095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582367-C-T

119157154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582310-T-G

119157173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582275-G-T

119157185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582263-T-C

119157185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582263-T-G

http://identifiers.org/hco/12/GRCh38#119157187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116582261-C-A

119157263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582180-G-T

119157305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582139-T-C

119157305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582139-T-G

119157314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582130-T-G

119157334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582118-A-G

119157408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582087-G-A

119157421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582074-G-A

119157421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582074-G-T

119157437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582056-T-C

119157438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116582055-A-T

119157531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581967-G-A

http://identifiers.org/hco/12/GRCh38#119157535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116581963-C-A

119157535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581963-C-T

http://identifiers.org/hco/12/GRCh38#119157588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116581942-C-A

119157680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581845-C-T

http://identifiers.org/hco/12/GRCh38#119157794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116581732-C-A

119157794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581732-C-T

http://identifiers.org/hco/12/GRCh38#119157846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116581679-C-A

119157846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581679-C-T

http://identifiers.org/hco/12/GRCh38#119157850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116581675-C-A

119157850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581675-C-T

119157899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581632-G-A

119157899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581632-G-T

119157996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581526-T-A

119157996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581526-T-C

119158025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581498-A-G

119158081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581426-A-G

119158156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581336-G-A

119158202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581290-T-C

119158271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581222-G-A

119158271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581222-G-T

http://identifiers.org/hco/12/GRCh38#119158413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116581090-C-A

119158500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581013-G-T

119158508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116581005-T-C

119158591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580943-A-G

119158601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580933-G-A

119158611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580920-T-C

119158650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580881-G-A

119158671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580861-C-T

119158684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580848-T-A

http://identifiers.org/hco/12/GRCh38#119158695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116580837-C-A

119158695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580837-C-G

119158719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580811-T-C

119158837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580684-G-T

119159051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580477-T-A

119159051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580477-T-C

119159140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580391-T-C

http://identifiers.org/hco/12/GRCh38#119159149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116580382-C-A

119159149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580382-C-T

119159240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580295-T-C

119159278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580251-A-G

119159291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580236-T-C

119159501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580068-T-C

119159510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580059-A-G

119159545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116580032-A-G

119159648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116579897-C-G

119159648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116579897-C-T

http://identifiers.org/hco/12/GRCh38#119159684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116579865-C-A

119159708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116579837-C-T

119159759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116579770-G-T

http://identifiers.org/hco/12/GRCh38#119159791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116579737-C-A

119159814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116579715-C-T

http://identifiers.org/hco/12/GRCh38#119159834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116579695-C-A

119159855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116579675-A-G

119159876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116579654-A-T

http://identifiers.org/hco/12/GRCh38#119159930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116579608-C-A

119159985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116579553-A-G

http://identifiers.org/hco/12/GRCh38#119159992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116579546-C-A

http://identifiers.org/hco/12/GRCh38#119160067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116579470-C-A

http://identifiers.org/hco/12/GRCh38#119160173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116579375-C-A

119160254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116579256-T-C

119160284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116579212-T-C

119160301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116579157-C-G

http://identifiers.org/hco/12/GRCh38#119160324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116579134-A-C

119160324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116579134-A-G

119160324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116579134-A-T

119160373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116579073-C-T

119160485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116578961-A-G

http://identifiers.org/hco/12/GRCh38#119160509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116578900-C-A

119160509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116578900-C-G

119160509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116578900-C-T

119160558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116578853-G-T

119160618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116578793-G-A

119160680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116578731-G-T

119160899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116578525-T-C

119160899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116578525-T-G

http://identifiers.org/hco/12/GRCh38#119161082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116578341-A-C

119161154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116578202-T-C

119161220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116578041-T-C

119161226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116578035-A-G

119161302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577973-T-C

119161384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577898-G-A

119161384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577898-G-T

http://identifiers.org/hco/12/GRCh38#119161392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116577886-C-A

119161392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577886-C-T

119161415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577863-G-T

http://identifiers.org/hco/12/GRCh38#119161444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116577834-A-C

119161444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577834-A-G

119161444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577834-A-T

119161501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577715-G-A

119161736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577477-G-C

119161736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577477-G-T

119161967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577267-C-G

119161969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577265-A-T

119162026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577221-A-G

119162026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577221-A-T

119162108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577142-G-A

119162123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577128-G-A

119162124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116577127-A-G

http://identifiers.org/hco/12/GRCh38#119162327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116576449-A-C

119162335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116576441-T-A

http://identifiers.org/hco/12/GRCh38#119162372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116576406-C-A

119162534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116576248-A-G

http://identifiers.org/hco/12/GRCh38#119162577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116576207-C-A

119162585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116576199-A-G

119162612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116576172-G-T

119162630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116576154-A-T

119162739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116576063-G-A

119162767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116576035-A-G

119162902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116575900-C-T

119162959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116575874-A-G

119163010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29389
most severe consequence: 3 prime UTR variant
orthologous variants: 116575822-T-C