8537547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8210693-T-C

8537559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8210703-C-T

8537563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8210707-A-G

8537582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8210726-T-C

http://identifiers.org/hco/16/GRCh38#8537817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost
orthologous variants: http://identifiers.org/mco/16/GRCm39#8210931-C-A

http://identifiers.org/hco/16/GRCh38#8537900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#8211017-C-A

8537945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8211099-G-A

8537945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8211099-G-T

8538339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8211593-G-T

http://identifiers.org/hco/16/GRCh38#8538380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8211627-C-A

8538496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8211739-T-C

8538496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8211739-T-G

8538501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8211744-G-T

8539133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8212278-G-C

8539182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8212313-T-C

http://identifiers.org/hco/16/GRCh38#8541520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8213545-C-A

8541520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8213545-C-G

8541520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8213545-C-T

8541541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8213565-C-T

8541563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8213587-C-T

8541614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8213640-A-G

8541671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8213697-A-G

8542328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8213933-T-C

8542328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8213933-T-G

8542357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8213963-T-C

8542420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8214875-A-G

8542443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8214897-C-T

8542445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8214899-C-T

8542473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8214927-C-G

8542553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8215004-G-A

8542629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8215073-G-A

8542629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8215073-G-T

http://identifiers.org/hco/16/GRCh38#8542642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8215411-A-C

8542677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8215440-G-C

http://identifiers.org/hco/16/GRCh38#8542822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8215593-C-A

8542822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8215593-C-T

8542863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8215634-C-G

8542863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8215634-C-T

8542973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8215744-T-A

8543003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8215774-C-T

http://identifiers.org/hco/16/GRCh38#8543192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8215940-C-A

8543307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216055-C-T

8543341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216089-T-C

8543634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216945-A-G

8543634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216945-A-T

8543677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8216988-C-T

8543716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8217025-G-T

8543790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8217093-T-C

8544465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8217761-C-T

8544481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8217785-A-G

8544481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8217785-A-T

8544556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8217857-C-T

8544647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8217925-C-G

8566683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8223892-T-C

8566704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8223907-T-A

http://identifiers.org/hco/16/GRCh38#8566709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8223911-C-A

8566855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224017-G-A

8567330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8224381-G-A

8567330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8224381-G-C

8567344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224396-T-C

8567443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224470-G-A

8567461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8224488-G-T

8567859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8224757-C-T

8567860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8224758-A-G

8567906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8224796-A-G

8568026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8224906-A-G

8568409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8225224-T-C

8568478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8225281-T-C

8568686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8225982-C-T

8569434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227072-G-A

8569434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227072-G-T

http://identifiers.org/hco/16/GRCh38#8569462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8227100-A-C

8569462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227100-A-G

8569463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227101-G-A

8569463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227101-G-C

8569463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227101-G-T

8569535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227172-G-A

8569535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227172-G-C

8569535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227172-G-T

8569561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227194-A-G

http://identifiers.org/hco/16/GRCh38#8569569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8227205-C-A

8569569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227205-C-G

8569569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227205-C-T

8569580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227216-G-A

8569580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227216-G-T

http://identifiers.org/hco/16/GRCh38#8569616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8227273-C-A

8569616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227273-C-G

8569616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227273-C-T

8569659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227300-T-C

8569671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227312-C-G

8569671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227312-C-T

8569675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227316-G-C

8569675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8227316-G-T

8569914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 8227534-G-A

8569914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 8227534-G-T

http://identifiers.org/hco/16/GRCh38#8569968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8227588-C-A

8569968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 8227588-C-T

8570028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227647-G-A

8570028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227647-G-T

8570072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227709-T-A

8570072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227709-T-C

http://identifiers.org/hco/16/GRCh38#8570076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8227713-C-A

8570076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227713-C-G

8570076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8227713-C-T

8571357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229273-T-A

8571397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229305-C-G

8571397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229305-C-T

8571523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229441-A-G

8571523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229441-A-T

8571609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229525-T-C

8571660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229572-A-G

8571819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229687-T-C

8571832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229712-T-C

8571918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229803-A-T

8572026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229908-C-G

8572026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229908-C-T

http://identifiers.org/hco/16/GRCh38#8572031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8229913-C-A

8572031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229913-C-T

8572059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8229938-C-T

http://identifiers.org/hco/16/GRCh38#8572109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8229987-A-C

8572109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 8229987-A-T

8572121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 8229999-G-A

8572121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 8229999-G-T

8572150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 8230028-G-A

8572311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8230186-G-A

8572311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8230186-G-C

8581897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8235208-G-A

8581912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8235223-A-G

8581912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8235223-A-T

8581916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8235227-A-G

8582003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8235310-C-T

8582110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8235403-T-C

8582418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8235698-T-C

8585637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8238727-A-G

http://identifiers.org/hco/16/GRCh38#8585765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8238856-A-C

8585791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8238883-G-A

8585791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8238883-G-C

http://identifiers.org/hco/16/GRCh38#8585914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8239184-A-C

8585914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8239184-A-G

8586177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8239418-A-G

8586841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8239953-A-G

8586897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8240006-C-T

8586958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8240065-A-G

8586959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8240066-C-T

8586964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8240071-C-G

8587048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8240140-G-A

8587345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8240565-T-C

8587503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8240722-C-G

8588201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8241010-C-T

8588325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8241112-A-G

8588341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8241132-A-G

8588341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8241132-A-T

8588408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8241194-G-C

8588532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8241312-C-T

8588687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8241465-T-C

8588784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8241510-C-T

8588916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8241658-G-C

8588923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8241665-T-C

8588935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8241677-G-A

8588964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8241713-T-C

http://identifiers.org/hco/16/GRCh38#8589081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8241810-C-A

8589081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8241810-C-T

8589170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8241896-A-G

8589327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8242039-C-T

http://identifiers.org/hco/16/GRCh38#8589354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8242066-C-A

8589354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8242066-C-T

8589359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8242071-G-A

8589359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8242071-G-T

8589445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8242150-T-C

8589506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8242208-T-C

8589524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8242226-G-A

http://identifiers.org/hco/16/GRCh38#8589537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8242239-C-A

8589537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8242239-C-T

8589604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8242285-G-A

8589604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8242285-G-C

8589604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8242285-G-T

8589610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8242291-C-T

8589647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8242328-G-A

http://identifiers.org/hco/16/GRCh38#8589665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8242346-C-A

8589665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8242346-C-G

8589665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8242346-C-T

http://identifiers.org/hco/16/GRCh38#8589685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8242366-C-A

8589685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8242366-C-T

8589697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 8242375-G-A

8589697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8242375-G-T

8589700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 8242378-C-G

8589700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 8242378-C-T

8589734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8242412-A-T

8589764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 8242442-G-A

8589764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 8242442-G-T

http://identifiers.org/hco/16/GRCh38#8589806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8242484-C-A

8589806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8242484-C-G

8589925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8242573-G-A

http://identifiers.org/hco/16/GRCh38#8590023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#8242614-C-A

8590023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8242614-C-T

http://identifiers.org/hco/16/GRCh38#8590059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#8242644-C-A

8590059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8242644-C-G

8590059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8242644-C-T

8590067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8242652-T-C

8590067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8242652-T-G

http://identifiers.org/hco/16/GRCh38#8590178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#8242716-C-A

8590178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 8242716-C-T

http://identifiers.org/hco/16/GRCh38#8590191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#8242728-C-A

8590242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5 prime UTR variant
orthologous variants: 8242765-G-A

8590242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5 prime UTR variant
orthologous variants: 8242765-G-T

http://identifiers.org/hco/16/GRCh38#8590253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8242774-C-A

http://identifiers.org/hco/16/GRCh38#8590307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8242834-A-C

8590307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5 prime UTR variant
orthologous variants: 8242834-A-G

8590307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5 prime UTR variant
orthologous variants: 8242834-A-T

http://identifiers.org/hco/16/GRCh38#8590330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#8242848-A-C

8590330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5 prime UTR variant
orthologous variants: 8242848-A-G

8590338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5 prime UTR variant
orthologous variants: 8242856-T-G

8590390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33227
most severe consequence: 5 prime UTR variant
orthologous variants: 8242893-G-T