81332264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83272323-C-T

81332747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 83271825-T-G

81332897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 83271675-C-G

81332897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 83271675-C-T

81332972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 83271600-A-G

81333073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 83271499-G-A

81333098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 83271474-A-G

81333098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 83271474-A-T

81333351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83271254-G-T

81333369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83271236-G-C

81333369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83271236-G-T

81333391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83271224-G-A

81333391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83271224-G-C

81333391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83271224-G-T

81333392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83271223-G-A

81333392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83271223-G-T

http://identifiers.org/hco/15/GRCh38#81333401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83271214-C-A

81333401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83271214-C-T

81333548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83271086-G-C

81333640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83271000-T-G

81334479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83269589-T-C

81334486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83269582-G-C

http://identifiers.org/hco/15/GRCh38#81334649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83269437-C-A

81334649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83269437-C-T

81334657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83269429-G-T

81334852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 83269228-G-A

81335029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83269076-A-G

81335402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83268366-T-G

http://identifiers.org/hco/15/GRCh38#81335585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83268195-C-A

http://identifiers.org/hco/15/GRCh38#81335835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83267887-C-A

81335835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83267887-C-T

http://identifiers.org/hco/15/GRCh38#81335848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83267799-C-A

81335848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83267799-C-T

81335867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83267772-C-G

81335958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83267656-G-A

81335958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83267656-G-T

81336066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83267554-T-G

81336134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83267492-G-A

81336134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83267492-G-C

http://identifiers.org/hco/15/GRCh38#81336239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83267423-C-A

81336239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83267423-C-G

81336239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83267423-C-T

81336893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83267098-T-C

81337405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83266387-T-C

81337405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83266387-T-G

81337490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83266296-A-G

81337494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83266292-G-T

81337505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83266283-T-C

81337505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83266283-T-G

http://identifiers.org/hco/15/GRCh38#81337545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83266252-C-A

http://identifiers.org/hco/15/GRCh38#81337582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83266229-C-A

81337582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83266229-C-T

http://identifiers.org/hco/15/GRCh38#81337647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83266216-C-A

81337647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83266216-C-G

81337651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83266212-G-A

http://identifiers.org/hco/15/GRCh38#81337696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83266167-C-A

81337696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83266167-C-T

81337699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83266164-C-T

81337722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83266141-A-G

81337807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83266058-G-A

81337807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83266058-G-T

81337891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 83265972-C-T

http://identifiers.org/hco/15/GRCh38#81337892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83265971-C-A

81337892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83265971-C-T

81337943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83265920-G-A

81337943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83265920-G-T

81337952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83265911-G-A

81337952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83265911-G-T

81337962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83265899-A-G

81338067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83265817-A-G

81338359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83265530-C-G

81338360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83265529-C-G

81338576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83265366-T-C

81338721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83265123-C-G

81338721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 83265123-C-T

81338798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83265045-A-G

http://identifiers.org/hco/15/GRCh38#81338903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#83264883-C-A

81338903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83264883-C-G

81338958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83264828-G-A

81338969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83264818-G-A

81339087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83264703-G-A

81339087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83264703-G-T

81339272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83264451-G-A

81339272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83264451-G-C

81339272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83264451-G-T

81339336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83264413-T-C

81339383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83264342-A-G

81339388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83264337-A-G

http://identifiers.org/hco/15/GRCh38#81339457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83264166-C-A

81339457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83264166-C-T

81339520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83264103-A-T

81339536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83264086-T-G

81339545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83264077-A-G

81339559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83263974-G-C

81339559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83263974-G-T

81339636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83263707-A-G

http://identifiers.org/hco/15/GRCh38#81339741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83263609-C-A

81339857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83263494-A-G

81339915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83263437-C-T

81339969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83263385-T-C

81340232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83262923-C-G

81340234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83262921-C-G

81340305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83262777-G-A

81340342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83262739-G-C

81340445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83262626-G-C

81341250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83261879-A-G

http://identifiers.org/hco/15/GRCh38#81341370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83261788-C-A

81341477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83261681-A-T

81341615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83261547-G-T

http://identifiers.org/hco/15/GRCh38#81341641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83261522-C-A

81341690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83261475-A-G

81341690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83261475-A-T

81341694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83261471-G-C

81341694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83261471-G-T

81341775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83261422-G-A

http://identifiers.org/hco/15/GRCh38#81341807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83261388-C-A

81341807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83261388-C-T

81341810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83261385-A-G

81341929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83261263-G-A

81342063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83261135-T-G

81342249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260939-C-T

81342364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260856-C-G

81342370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260850-A-G

http://identifiers.org/hco/15/GRCh38#81342415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83260815-A-C

81342598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260705-C-T

81342630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260673-T-C

http://identifiers.org/hco/15/GRCh38#81342667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83260637-A-C

81342667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260637-A-G

81342712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260597-A-G

81342713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260596-G-T

81342736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260572-A-G

http://identifiers.org/hco/15/GRCh38#81342786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83260475-C-A

81342786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260475-C-T

81342794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260467-G-A

81342794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260467-G-T

81342815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260446-C-T

81342917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260352-G-A

81342917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260352-G-T

81342935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260333-C-T

http://identifiers.org/hco/15/GRCh38#81343233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83260027-C-A

81343256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83260006-A-G

81343270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83259993-A-T

81343433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83259830-T-G

81343455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83259808-A-G

81343527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83259664-T-C

81344031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 83259064-G-A

81344031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 83259064-G-C

81344031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 83259064-G-T

http://identifiers.org/hco/15/GRCh38#81344161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83258920-C-A

http://identifiers.org/hco/15/GRCh38#81344657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83258630-C-A

81344684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83258600-G-A

81344684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83258600-G-C

81344684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83258600-G-T

81344686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83258598-G-A

81344686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83258598-G-T

http://identifiers.org/hco/15/GRCh38#81344836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83258460-A-C

81344836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83258460-A-G

81344842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83258454-G-T

81344872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83258424-T-G

81345013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 83258242-T-C

81345013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 83258242-T-G

81345032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83258223-A-G

81345035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83258220-G-T

81345039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83258216-G-C

81345055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83258200-G-A

81345061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83258194-G-A

81345073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83258182-A-G

81345315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83257810-C-T

81345512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83257629-G-C

81346312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83257060-G-A

81346312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83257060-G-T

http://identifiers.org/hco/15/GRCh38#81346346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83257032-A-C

81346346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83257032-A-G

81346347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83257031-T-C

http://identifiers.org/hco/15/GRCh38#81346539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83256844-A-C

81346539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83256844-A-G

81346539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83256844-A-T

81346540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83256843-T-C

81346549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83256834-T-C

81346584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83256705-G-C

81346584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83256705-G-T

81346622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83256540-G-C

81346626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83256536-G-T

81346664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83256503-A-T

81346811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83256377-C-T

81347047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83256160-C-G

81347120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83256095-T-C

http://identifiers.org/hco/15/GRCh38#81347442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83255617-A-C

http://identifiers.org/hco/15/GRCh38#81347955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83255090-C-A

81348147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83254908-A-G

81348446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83254652-A-G

81348517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83254589-T-C

81348781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83254361-C-T

http://identifiers.org/hco/15/GRCh38#81349336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83254163-A-C

81349336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83254163-A-G

81349560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83253944-A-T

81349599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83253917-T-C

81349600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83253916-T-C

http://identifiers.org/hco/15/GRCh38#81349613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83253903-C-A

81349613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83253903-C-G

81349613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83253903-C-T

http://identifiers.org/hco/15/GRCh38#81349615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83253901-C-A

81349689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83253823-T-A

81349689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83253823-T-C

81349723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83253785-A-G

81349723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83253785-A-T

81349786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83253730-C-T

http://identifiers.org/hco/15/GRCh38#81349790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83253726-A-C

81349790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83253726-A-T

81350597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83253361-A-T

81350721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83253253-T-C

81350971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83253045-T-C

http://identifiers.org/hco/15/GRCh38#81351755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83252620-A-C

81351755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83252620-A-G

http://identifiers.org/hco/15/GRCh38#81351908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83252502-A-C

http://identifiers.org/hco/15/GRCh38#81351934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83252476-C-A

81351934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83252476-C-T

http://identifiers.org/hco/15/GRCh38#81351977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83252449-C-A

81351977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83252449-C-G

http://identifiers.org/hco/15/GRCh38#81351981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83252445-C-A

81351981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83252445-C-G

81351981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83252445-C-T

81352024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83252420-T-C

81354745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83251563-G-T

81354900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83251408-T-C

81355579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83250270-G-T

81355659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83250192-A-G

http://identifiers.org/hco/15/GRCh38#81355684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83250164-A-C

81355686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83250162-C-T

81355710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83250150-A-G

http://identifiers.org/hco/15/GRCh38#81355787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83250072-C-A

81355787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83250072-C-T

81356006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249679-T-A

81356254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249461-A-G

81356335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249385-G-A

81356335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249385-G-T

81356336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249384-A-G

http://identifiers.org/hco/15/GRCh38#81356366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83249368-C-A

81356400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249343-A-G

http://identifiers.org/hco/15/GRCh38#81356418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83249323-C-A

81356418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249323-C-T

http://identifiers.org/hco/15/GRCh38#81356528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83249220-C-A

81356528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 83249220-C-T

81356574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83249174-G-A

http://identifiers.org/hco/15/GRCh38#81356620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83249129-C-A

81356620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249129-C-T

http://identifiers.org/hco/15/GRCh38#81356657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83249091-C-A

81356657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249091-C-T

http://identifiers.org/hco/15/GRCh38#81356692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83249059-C-A

81356692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249059-C-G

81356692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249059-C-T

81356707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249049-G-A

81356707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249049-G-T

81356717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249039-G-A

81356717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249039-G-C

81356717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249039-G-T

81356719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249037-G-A

81356719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249037-G-T

81356722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249035-A-G

81356737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83249020-G-A

81356856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83248899-G-T

81356867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83248890-C-T

http://identifiers.org/hco/15/GRCh38#81356905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83248859-A-C

81356938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83248833-T-G

81357004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83248757-C-T

81357238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83248536-A-T

81357367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83248397-A-G

81357536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83248213-C-T

http://identifiers.org/hco/15/GRCh38#81357617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83248107-C-A

81357661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83248073-C-T

81358524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83247382-A-G

81358561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83247350-G-A

81358561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83247350-G-T

81358566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83247345-G-T

81358663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83247246-G-T

81358833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83247095-G-A

81359110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83246961-C-T

81359128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83246940-C-T

81359156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83246915-G-A

81359225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83246878-T-C

81359331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83246805-T-C

81359340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83246796-G-A

81359340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83246796-G-T

81359387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83246737-C-T

http://identifiers.org/hco/15/GRCh38#81359420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83246704-A-C

81359420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83246704-A-T

81359422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83246702-T-A

81359453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83246671-A-G

81359473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 83246651-T-C

81359567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83246577-G-A

81359567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83246577-G-T

81359595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83246547-T-A

81359725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83246440-G-A

81359725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83246440-G-C

81361258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83245769-G-T

http://identifiers.org/hco/15/GRCh38#81362015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83245545-C-A

81362015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245545-C-T

81362016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245544-G-A

81362016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245544-G-C

81362016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245544-G-T

81362031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245529-A-G

http://identifiers.org/hco/15/GRCh38#81362157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83245409-C-A

81362157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245409-C-T

81362188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245380-T-G

http://identifiers.org/hco/15/GRCh38#81362203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83245365-C-A

81362203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245365-C-T

81362293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 83245275-C-T

81362313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245255-G-T

http://identifiers.org/hco/15/GRCh38#81362377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83245184-A-C

81362421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245142-A-G

81362421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245142-A-T

http://identifiers.org/hco/15/GRCh38#81362425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83245138-C-A

81362425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245138-C-G

81362425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245138-C-T

http://identifiers.org/hco/15/GRCh38#81362434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83245129-C-A

81362450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245114-G-A

81362450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245114-G-T

81362458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83245106-G-T

81362810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83244667-A-G

81362835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83244642-T-C

81362851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83244631-G-C

81362887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83244595-C-T

81362918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83244557-G-C

81362965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83244510-C-G

81363435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83244341-G-T

81363536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83244240-G-C

81363642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83244144-C-T

81363913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83243913-T-A

81364105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83243732-G-A

81364324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83242862-G-A

81366505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83241584-T-C

81366792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83241126-C-T

81366801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83241117-T-C

81366929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83241027-T-C

81367166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83240676-T-C

81367256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83240596-T-C

81367343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83240515-G-A

81367387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83240478-T-A

81367387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83240478-T-G

81367484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83240364-A-T

81367539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83240304-A-T

81367683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83240159-A-G

81367733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83240105-A-G

81367790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83240046-T-C

81367796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83240040-C-G

81367800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83240037-A-G

81367803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83240034-A-T

81368368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83239806-A-G

http://identifiers.org/hco/15/GRCh38#81368660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#83239473-A-C

81370370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83237354-G-A

81370377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83237347-T-C

81371631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83236880-C-T

81371824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83236590-A-T

81372264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83236185-G-C

81372594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83235635-A-G

81372603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83235626-A-G

81372817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22995
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83235414-T-G