232632419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191206-T-C

232632491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191279-T-C

232633148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191628-C-T

http://identifiers.org/hco/2/GRCh38#232633162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87191642-A-C

232633162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191642-A-G

http://identifiers.org/hco/2/GRCh38#232633174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87191647-A-C

232633174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191647-A-G

232633174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191647-A-T

232633246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191716-G-A

232633246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191716-G-T

232633324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191789-G-A

232633324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191789-G-C

232633324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191789-G-T

http://identifiers.org/hco/2/GRCh38#232633342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87191815-C-A

232633342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191815-C-T

http://identifiers.org/hco/2/GRCh38#232633377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87191870-C-A

232633377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191870-C-T

http://identifiers.org/hco/2/GRCh38#232633417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87191909-C-A

232633417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191909-C-T

232633453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191944-G-A

232633453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191944-G-C

http://identifiers.org/hco/2/GRCh38#232633492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87191973-C-A

232633492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191973-C-T

232633496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191977-C-T

232633505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87191986-A-G

232633585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87192058-G-A

232633585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87192058-G-C

232633585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: intron variant
orthologous variants: 87192058-G-T

232633621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87192094-C-G

232633621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87192094-C-T

http://identifiers.org/hco/2/GRCh38#232633647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87192120-C-A

232633647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87192120-C-G

232633647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87192120-C-T

232633669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87192138-G-A

http://identifiers.org/hco/2/GRCh38#232633676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87192145-C-A

232633676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87192145-C-G

232633676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87192145-C-T

http://identifiers.org/hco/2/GRCh38#232633703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87192170-C-A

232633703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87192170-C-T

232633917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 87192387-G-A

232633917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 87192387-G-T

232633923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 87192393-G-A

http://identifiers.org/hco/2/GRCh38#232633926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87192396-C-A

232633926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 87192396-C-T

http://identifiers.org/hco/2/GRCh38#232633929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#87192399-C-A

232633929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 87192399-C-G

232633929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 87192399-C-T

232633959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 87192429-G-A

232633959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 87192429-G-T

232634031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87192494-G-A

232634031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87192494-G-T

232634055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87192527-G-A

232634055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87192527-G-T

232634143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87192614-T-A

232634143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87192614-T-C

232634145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87192616-T-G

232634575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87193009-C-T

232634580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87193014-A-G

232634580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87193014-A-T

232634585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87193019-G-C

232634665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87193131-G-A

232635082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87193848-C-T

http://identifiers.org/hco/2/GRCh38#232635138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87193898-A-C

232635138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87193898-A-G

232635413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87194148-G-A

232636856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87197205-C-T

232636906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87197265-C-G

232636979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87197354-G-T

232637689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87198172-C-T

232637690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87198173-G-A

232637706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87198189-C-T

232637799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87198290-T-G

232637942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87198441-A-G

http://identifiers.org/hco/2/GRCh38#232638083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87198569-C-A

232638084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87198570-T-C

232638094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87198580-G-T

232638140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87198630-G-A

232638140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87198630-G-T

http://identifiers.org/hco/2/GRCh38#232638304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87198798-C-A

232638325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87198822-C-T

232638380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87198877-T-A

232638529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87199018-C-T

232638573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87199128-A-G

232638598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87199206-T-C

232638598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87199206-T-G

232638658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87199293-G-A

http://identifiers.org/hco/2/GRCh38#232638672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87199313-A-C

232638672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87199313-A-G

232638674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87199315-A-G

232638720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87199366-G-T

232638803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87199480-G-A

232638880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87199558-T-C

232638886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87199564-G-C

232638917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87199588-A-G

232643363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87200013-G-A

232645287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87201285-G-A

232645496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87201476-C-T

232645598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87201574-C-T

232645755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87201724-A-G

http://identifiers.org/hco/2/GRCh38#232645811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87201781-C-A

232645891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87201838-G-A

232645971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87201903-C-T

232646012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87201923-G-A

232646120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87202005-C-G

232646160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87202044-G-A

http://identifiers.org/hco/2/GRCh38#232646479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87202381-C-A

232646620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87202569-T-C

232646620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87202569-T-G

232646699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87202666-G-A

232646699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87202666-G-T

232646743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87202697-G-A

232646784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87202726-A-G

232646837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87202805-C-T

232646929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87202889-C-T

232647108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87203039-C-T

232647109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87203040-A-G

232647149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87203080-A-G

232647397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87203333-C-T

232647600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87203494-T-G

232648223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87205115-C-T

232648632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87205471-G-A

232648647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87205486-T-C

232648674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87205514-G-A

232648767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87205582-C-T

232648792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87205606-G-C

232648929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87205866-T-A

232649386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87206187-A-G

232649801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87206550-A-G

232649807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87206561-G-C

http://identifiers.org/hco/2/GRCh38#232652045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87208258-C-A

232652186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87208399-T-A

232652189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87208402-C-T

232652221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87208436-C-T

232652373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87208591-A-G

http://identifiers.org/hco/2/GRCh38#232655112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87211237-C-A

232655486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87211510-C-T

232658407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87213137-C-T

232658520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87213248-T-C

232658572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87213296-A-G

232659178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87214861-C-T

http://identifiers.org/hco/2/GRCh38#232659232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87214905-A-C

232659232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87214905-A-G

232659294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87214935-A-G

232659295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87214936-A-T

232659343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87214962-T-C

232659343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87214962-T-G

232659510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87215092-G-A

http://identifiers.org/hco/2/GRCh38#232660698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87215331-C-A

232661091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87215612-T-C

232661103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87215624-G-A

232661103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87215624-G-C

232661111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87215633-T-G

232661208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87215748-T-C

232661254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87215778-C-T

232661493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87215975-G-C

232661776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87216252-T-C

http://identifiers.org/hco/2/GRCh38#232661784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87216259-C-A

http://identifiers.org/hco/2/GRCh38#232661837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87216296-A-C

232661837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87216296-A-G

232661837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87216296-A-T

232661954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87216322-C-G

http://identifiers.org/hco/2/GRCh38#232662020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87216404-C-A

232662030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87216417-G-A

232662030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87216417-G-T

232662047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87216438-T-C

232662170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87216570-T-C

232662279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87216674-A-T

232662303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87216706-G-A

232662719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87217108-A-G

232662762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87217151-T-C

232662763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87217152-G-A

http://identifiers.org/hco/2/GRCh38#232662829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#87217217-C-A

232662829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 87217217-C-T

232662928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87217316-T-C

232662999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87217367-C-T

232663035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87217400-T-C

232663049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87217413-G-A

232663054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87217422-G-A

232663054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87217422-G-C

http://identifiers.org/hco/2/GRCh38#232663068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87217436-C-A

232663068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87217436-C-G

232663068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87217436-C-T

232666525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87217836-G-A

232666785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87218097-G-A

232667678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87218896-A-G

232667692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87218909-A-G

232667697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87218914-C-T

232667701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87218918-C-T

232667793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87219073-G-A

232667904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87219167-A-G

http://identifiers.org/hco/2/GRCh38#232668035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87219297-A-C

232668183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87219433-C-G

232669200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87220713-C-T

232669345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87220887-C-T

232669352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87220894-T-C

http://identifiers.org/hco/2/GRCh38#232669602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87221083-C-A

232669602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87221083-C-T

232669627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87221111-G-A

232669627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87221111-G-T

232669710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87221183-C-T

232669726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87221199-G-T

232669745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87221217-C-T

232669757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87221230-C-T

232669759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87221232-C-T

232670825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87222986-A-G

232671113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87223201-G-A

232672507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87225547-G-A

232672554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87226721-A-G

232672573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87226740-T-C

232672938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87227113-C-G

232673389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87227404-G-A

232673514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87227535-G-T

232673616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87227638-T-C

http://identifiers.org/hco/2/GRCh38#232673721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87227743-A-C

232673721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87227743-A-G

232674593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87228168-G-A

232674669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87228241-G-C

232674819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87228391-G-A

232674864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87228435-G-A

232674864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87228435-G-T

232676215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87229077-T-G

232676282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87229139-C-T

232676378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87229190-C-T

232676553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87229328-C-T

232676579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87229354-C-T

232676671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87229434-G-A

232676671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87229434-G-T

232676754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87229502-G-A

http://identifiers.org/hco/2/GRCh38#232681470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87237273-C-A

232681470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87237273-C-T

232681501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87237299-T-A

232681560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87237360-G-A

232681602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87237400-G-A

http://identifiers.org/hco/2/GRCh38#232681758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87237555-C-A

http://identifiers.org/hco/2/GRCh38#232681836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87237634-C-A

http://identifiers.org/hco/2/GRCh38#232681866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87237683-A-C

232681866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: 87237683-A-T

http://identifiers.org/hco/2/GRCh38#232681885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87237702-C-A

232681885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: 87237702-C-T

232681946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: 87237744-T-C

232682100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: 87237872-T-C

http://identifiers.org/hco/2/GRCh38#232682101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87237873-C-A

232682101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: 87237873-C-G

232682101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: 87237873-C-T

http://identifiers.org/hco/2/GRCh38#232682132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87237904-C-A

232682174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: 87237943-T-C

http://identifiers.org/hco/2/GRCh38#232682265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87238038-C-A

232682265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: 87238038-C-G

232682265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: 87238038-C-T

232682519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29556
most severe consequence: 3 prime UTR variant
orthologous variants: 87238229-G-A