463357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475357-G-A

463357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475357-G-C

463357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475357-G-T

463365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475364-G-T

463407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475405-G-A

463407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475405-G-T

463430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475428-G-A

463430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475428-G-C

463467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475450-A-G

463492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475472-G-A

463492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475472-G-T

http://identifiers.org/hco/19/GRCh38#463537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79475508-A-C

463537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475508-A-G

463537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475508-A-T

463654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475579-G-A

463654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475579-G-T

463725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475646-G-A

463725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475646-G-C

463730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 3 prime UTR variant
orthologous variants: 79475651-G-A

463860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: missense variant
orthologous variants: 79475707-G-A

463860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: missense variant
orthologous variants: 79475707-G-C

463860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: missense variant
orthologous variants: 79475707-G-T

463927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: missense variant
orthologous variants: 79475776-G-A

463927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: missense variant
orthologous variants: 79475776-G-T

463970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: synonymous variant
orthologous variants: 79475819-G-A

463982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: synonymous variant
orthologous variants: 79475831-G-A

http://identifiers.org/hco/19/GRCh38#464039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79475888-C-A

464041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: missense variant
orthologous variants: 79475890-G-T

http://identifiers.org/hco/19/GRCh38#464063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79475912-C-A

464063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: synonymous variant
orthologous variants: 79475912-C-T

464390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79476235-G-A

464390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79476235-G-T

464666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79476450-C-T

http://identifiers.org/hco/19/GRCh38#464764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79476533-A-C

464984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79476818-G-A

464989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79476823-T-A

465035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79476862-A-G

465053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79476880-T-G

465260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477057-G-A

465260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477057-G-C

465260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477057-G-T

http://identifiers.org/hco/19/GRCh38#465277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79477074-A-C

465277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477074-A-G

465277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477074-A-T

465290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477088-G-C

465290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477088-G-T

465310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477109-G-T

465323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477122-A-G

465323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477122-A-T

465339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477138-G-A

465339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477138-G-T

465340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477139-T-A

465340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477139-T-G

465343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477142-A-G

465361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477160-G-A

465361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477160-G-C

465361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477160-G-T

465371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477170-A-G

465375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477174-A-G

465375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477174-A-T

465391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477190-A-G

465406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477205-G-T

465407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477206-G-A

465407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477206-G-T

465431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477230-G-A

465431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477230-G-C

465431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477230-G-T

465441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477240-G-A

465450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477249-A-G

465450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477249-A-T

465454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477253-G-A

465454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477253-G-C

465454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477253-G-T

465487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477286-G-A

465487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477286-G-C

465487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477286-G-T

465490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477289-A-G

465490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477289-A-T

465495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477294-A-G

465495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477294-A-T

http://identifiers.org/hco/19/GRCh38#465511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79477298-C-A

465511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477298-C-G

465515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477302-A-G

465527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477314-A-G

465535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477322-G-A

465535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477322-G-C

465535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477322-G-T

465536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477323-T-G

465551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477338-A-G

465554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477341-G-T

465555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477342-A-G

465555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477342-A-T

465556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477343-T-A

465558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477345-G-A

465558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477345-G-T

465568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477355-T-G

http://identifiers.org/hco/19/GRCh38#465580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79477367-C-A

465586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477373-G-C

465587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477374-G-A

465587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477374-G-T

465599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477386-A-G

465625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477406-G-A

465625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477406-G-C

465625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477406-G-T

465631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477412-G-A

465631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477412-G-T

465640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477421-G-A

465640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477421-G-T

465643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477424-G-A

465643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477424-G-T

465645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477426-G-A

465645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477426-G-C

465645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477426-G-T

465649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477430-A-G

465649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477430-A-T

http://identifiers.org/hco/19/GRCh38#465667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79477448-A-C

465667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477448-A-G

465667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477448-A-T

http://identifiers.org/hco/19/GRCh38#465727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79477504-A-C

465727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477504-A-G

465734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477511-A-G

465734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477511-A-T

465739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477516-G-A

465739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477516-G-C

465757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477534-G-A

465757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477534-G-C

465757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477534-G-T

465762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477539-T-A

465762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477539-T-G

465769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477546-G-A

465769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477546-G-C

465769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477546-G-T

465787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477564-G-A

465787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477564-G-C

465787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477564-G-T

465816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477593-A-G

465829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477606-A-G

465829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477606-A-T

465836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477614-A-G

465836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477614-A-T

465868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477646-G-A

465868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477646-G-T

465872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477650-A-G

465872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477650-A-T

465876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477654-G-A

465876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477654-G-C

465876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477654-G-T

465887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477665-G-A

465887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477665-G-T

465896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477674-A-G

465911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477689-G-A

465911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477689-G-C

465911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477689-G-T

465930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477708-G-A

465930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477708-G-C

465930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477708-G-T

465964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477739-T-A

465964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477739-T-G

465999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477774-G-A

465999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477774-G-C

465999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477774-G-T

466007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477779-T-A

466007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477779-T-G

466019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477791-T-A

466022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477794-A-G

466034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477806-G-A

466034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477806-G-C

466034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477806-G-T

466050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477822-G-A

466050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477822-G-C

466050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477822-G-T

466059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477831-T-A

466059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477831-T-C

466062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477834-G-A

466062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477834-G-C

466062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477834-G-T

466096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477837-G-A

466096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477837-G-C

http://identifiers.org/hco/19/GRCh38#466115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79477856-A-C

466115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477856-A-G

466123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477864-G-A

466123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477864-G-C

466123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477864-G-T

466136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477877-G-A

466136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477877-G-C

466136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477877-G-T

466141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477882-G-A

466141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477882-G-C

466141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477882-G-T

466156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477897-G-C

466156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477897-G-T

466274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477982-G-C

466281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477989-G-A

466283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477991-G-A

466283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79477991-G-T

466293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79478001-G-A

466301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79478009-G-A

466301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79478009-G-T

466372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79478076-G-A

466372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79478076-G-T

466392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79478096-G-A

466392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79478096-G-C

467653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79478418-A-G

467660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79478425-G-T

467689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79478454-G-A

469127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79479156-T-C

472357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79480412-T-A

472357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79480412-T-C

472357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79480412-T-G

http://identifiers.org/hco/19/GRCh38#472377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79480431-C-A

472377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79480431-C-T

http://identifiers.org/hco/19/GRCh38#472473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79480527-C-A

472473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79480527-C-G

472473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79480527-C-T

http://identifiers.org/hco/19/GRCh38#472671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79480684-C-A

472671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron variant
orthologous variants: 79480684-C-T

472726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron variant
orthologous variants: 79480736-A-T

472865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron variant
orthologous variants: 79480863-C-G

472992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron variant
orthologous variants: 79480994-G-C

472992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron variant
orthologous variants: 79480994-G-T

473709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron variant
orthologous variants: 20464925-G-A

473709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron variant
orthologous variants: 20464925-G-C

473982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron variant
orthologous variants: 79480994-G-C

http://identifiers.org/hco/19/GRCh38#474140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79481087-C-A

474480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron variant
orthologous variants: 79481287-G-T

474516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron variant
orthologous variants: 79481323-G-A

474585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron variant
orthologous variants: 79481372-A-G

http://identifiers.org/hco/19/GRCh38#474734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#79481514-C-A

474734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: intron_variant, missense_variant
orthologous variants: 79481514-C-T

474891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79481662-G-A

474891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79481662-G-C

474891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79481662-G-T

474916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79481687-C-G

474916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26841
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79481687-C-T