108129332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5 prime UTR variant
orthologous variants: 113638614-G-T

108130322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113639001-C-T

http://identifiers.org/hco/12/GRCh38#108130407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113639057-C-A

108130790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113639361-C-G

108130790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113639361-C-T

108130822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113639385-A-T

108130997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113639678-G-A

108131216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113639916-G-T

108131231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113639931-T-G

108131916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113640683-G-A

108131916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113640683-G-T

108131939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113640705-C-T

108131995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113640752-G-T

http://identifiers.org/hco/12/GRCh38#108132281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113640994-C-A

108132302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113641028-G-A

108132302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113641028-G-C

108132544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113641231-A-G

108132811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113641280-C-T

108132894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113641358-C-T

108132938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113641402-G-A

108133784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113642046-G-A

108133849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113642092-A-G

108134271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113642428-G-A

108134293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113642449-G-A

108134496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113643183-G-A

108134538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113643215-A-G

http://identifiers.org/hco/12/GRCh38#108134715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113643347-C-A

108134810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113643462-C-T

108134883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113643527-C-T

108134885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113643529-C-T

108134895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113643539-G-C

108135086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113643726-G-A

108135361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113644250-G-A

http://identifiers.org/hco/12/GRCh38#108135947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113644789-A-C

108136064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113644901-G-A

108136248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113645258-A-G

108136450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113645521-G-T

108136454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113645525-G-T

108136643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113645675-A-G

108136702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113645746-A-G

108137067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113646620-T-C

108137108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113646668-T-C

108140792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113649513-C-T

108140823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113649545-G-A

108140823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113649545-G-T

http://identifiers.org/hco/12/GRCh38#108140845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113649576-C-A

http://identifiers.org/hco/12/GRCh38#108140887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113649655-C-A

108140887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113649655-C-G

108140887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113649655-C-T

108142307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113651922-A-G

108142427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113652046-A-G

108151964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113658309-G-A

108152006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113658347-G-A

108152268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113658597-G-T

108152421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113658769-C-T

108152450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113658798-G-A

108152573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113658910-C-G

108152573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113658910-C-T

108153349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113659424-C-T

108153507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113659573-G-A

108153708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113659758-A-G

108153746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113659813-G-C

108155192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113660791-A-G

108155466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113661023-A-G

http://identifiers.org/hco/12/GRCh38#108155510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113661066-A-C

108155682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113661220-T-C

108155724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113661312-G-C

http://identifiers.org/hco/12/GRCh38#108155984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113661590-C-A

http://identifiers.org/hco/12/GRCh38#108155986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113661592-A-C

108156488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113662057-T-C

108156525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113662100-G-A

108156622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113662160-G-A

108158198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113663862-C-T

108160038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113664923-C-T

108160146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113665026-C-G

108160242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113665141-G-C

108165714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113668466-C-G

108165714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113668466-C-T

108165790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113668546-C-T

108165967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113668662-A-G

108165986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113668681-T-G

108166042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113668723-A-G

108166135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113668810-C-G

108166139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113668814-T-C

108166365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113669008-G-A

108170937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113674080-A-G

108170938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113674081-A-G

108171059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113674198-C-T

108175107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113674665-A-T

108175124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113674673-A-G

108175348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113674897-C-T

108175427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113674971-C-T

108175473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113675017-G-A

108175576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113675124-A-G

108175597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113675147-C-T

108175631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113675186-T-C

http://identifiers.org/hco/12/GRCh38#108175635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#113675190-A-C

108175635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113675190-A-T

108175658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113675213-G-A

108175722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113675256-G-A

108179564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113676439-A-G

108180089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113677006-G-A

108180089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113677006-G-T

108181032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113677874-A-G

108181140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113677988-C-T

108181218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113678066-C-T

108181272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113678117-G-C

108181766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113678537-C-T

108181839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113678642-G-A

108181872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113678669-T-A

108181872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113678669-T-C

108181928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113678695-C-T

108182233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113678989-G-A

108182298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113679053-T-C

108184920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 113680612-A-G

108185074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113680729-C-T

108185112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113680762-C-T

108185171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113680814-G-A

108185171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113680814-G-T

108185483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113680979-G-A

http://identifiers.org/hco/12/GRCh38#108185924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113681388-A-C

108191097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113682786-A-G

108191166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113682840-A-G

108191413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113683055-T-C

108191437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113683080-G-A

108191567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113683191-T-C

108191782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113683583-G-A

108191823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113683617-G-A

108191863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113683657-C-T

http://identifiers.org/hco/12/GRCh38#108191878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113683676-C-A

108191878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113683676-C-T

108193758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113686262-G-A

108193963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113686454-G-A

108194236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113686680-G-T

108194264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113686703-A-G

108194264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113686703-A-T

108194333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113686765-G-C

108194339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113686771-G-A

108194339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113686771-G-T

108194456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113686938-C-T

http://identifiers.org/hco/12/GRCh38#108195212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113688411-C-A

108195232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113688431-T-C

http://identifiers.org/hco/12/GRCh38#108195324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113688526-C-A

108195324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113688526-C-G

108195381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113688586-G-A

108195381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113688586-G-T

108195431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113688637-G-A

108195431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113688637-G-T

108195437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113688643-A-G

http://identifiers.org/hco/12/GRCh38#108195500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113688683-C-A

http://identifiers.org/hco/12/GRCh38#108195541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113688723-A-C

108195541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113688723-A-G

http://identifiers.org/hco/12/GRCh38#108195582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113688750-C-A

108195676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113688846-T-A

108195676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113688846-T-C

108195757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113688917-G-A

108195813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113688976-C-G

http://identifiers.org/hco/12/GRCh38#108195817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113688980-C-A

108195817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113688980-C-T

108195880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113689052-T-C

108195985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113689157-C-T

108196002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113689171-G-A

108196002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113689171-G-C

108196075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113689244-A-G

108196246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113689412-G-A

108196246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113689412-G-T

108196265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113689429-A-G

108196282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113689446-A-T

108196940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113690598-G-A

108196940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113690598-G-T

108196975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113690632-C-G

108196999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113690657-A-G

108197111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113690760-A-G

108197131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113690780-C-T

108197258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113690861-A-G

108197264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113690867-A-G

108197264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113690867-A-T

http://identifiers.org/hco/12/GRCh38#108197289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113690898-C-A

108197292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113690901-T-C

108197298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113690907-G-A

108197298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113690907-G-T

http://identifiers.org/hco/12/GRCh38#108197306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113690915-C-A

108197501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113691071-G-T

108197646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113691235-C-T

108198297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113691769-T-G

108198327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113691799-C-T

108198331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113691803-G-A

108198582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113692259-A-G

108198772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113692406-G-A

108198932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113692563-G-C

108201475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113693373-A-G

108201536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113693402-C-G

108201536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113693402-C-T

108201602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113693463-C-T

108201653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113693494-T-G

108201698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113693529-G-C

108201698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113693529-G-T

108201759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113693584-T-C

108201884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113693717-G-C

108201898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113693731-T-C

108201926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113693744-T-C

108201967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113693773-T-A

108201980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113693786-G-A

108202043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113693850-C-T

108202270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113694006-T-C

108202320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113694035-A-G

108202372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113694075-C-T

108204645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113694748-T-C

http://identifiers.org/hco/12/GRCh38#108204876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113694936-A-C

108204932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113694996-G-C

108205683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113695857-A-T

108205810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113695973-C-G

108206035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113696161-T-C

108206102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113696250-C-T

108206211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113696333-G-A

108206227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113696348-T-C

108206227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113696348-T-G

108206335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113696456-T-C

108206647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113697027-A-G

108209100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113697801-T-C

108209532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113698253-A-G

108209927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113698699-T-C

108209982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113698757-T-C

http://identifiers.org/hco/12/GRCh38#108209983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113698763-C-A

108209983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113698763-C-T

http://identifiers.org/hco/12/GRCh38#108209985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113698765-C-A

108209985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113698765-C-T

108210055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113698888-G-A

http://identifiers.org/hco/12/GRCh38#108210196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113699037-C-A

108210196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113699037-C-T

108210247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113699088-C-G

108210247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113699088-C-T

108210317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113699158-T-A

108210317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113699158-T-C

http://identifiers.org/hco/12/GRCh38#108210397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113699243-C-A

108210397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113699243-C-G

http://identifiers.org/hco/12/GRCh38#108210405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113699250-C-A

108210405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113699250-C-T

http://identifiers.org/hco/12/GRCh38#108210454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113699296-A-C

108210454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113699296-A-G

108210454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113699296-A-T

108211995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113700311-C-T

108212200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113700470-T-C

108212204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113700474-T-G

108212254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113700524-T-C

108212317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113700581-G-T

108212324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113700588-A-T

108212373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113700625-T-C

108213005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113701286-G-A

108213546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113701698-A-G

108213555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113701707-G-C

108213630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113701771-C-T

108213655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113701802-C-T

108213680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113701827-A-G

108213978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113702071-G-T

108214005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113702098-C-T

108214586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113702576-C-T

108214616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113702606-A-G

108214861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113702946-G-A

108215003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113703080-C-G

108215305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113703466-G-C

108215499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113703620-G-C

108215516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113703637-T-C

108215583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113703711-G-A

http://identifiers.org/hco/12/GRCh38#108215610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113703738-A-C

108215610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113703738-A-G

108215743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113703875-G-C

108215749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113703881-C-T

108215949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113704038-T-C

108215950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113704039-G-A

108216041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113704131-C-T

108216471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113704430-G-A

108217205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113704921-G-C

108217329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113704996-G-A

108217446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113705094-G-A

108217545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113705188-A-G

108217710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113705308-G-C

108217800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113705360-G-A

108217800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113705360-G-C

108217950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113705471-C-T

108218004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113705506-G-A

108224117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113707188-T-C

108224397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113707469-G-A

108224609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113707622-T-C

http://identifiers.org/hco/12/GRCh38#108224610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113707623-C-A

108224610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113707623-C-G

108224617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113707630-G-T

108224853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113708812-C-T

108224882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113708845-T-G

108224890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113708853-A-G

http://identifiers.org/hco/12/GRCh38#108226969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113710287-C-A

108226969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113710287-C-G

108227121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 113710431-C-T

108227183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113710491-C-T

http://identifiers.org/hco/12/GRCh38#108227277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113710558-A-C

108227293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113710578-T-A

108227293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113710578-T-C

108227301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113710586-T-C

http://identifiers.org/hco/12/GRCh38#108227302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113710587-C-A

108227302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113710587-C-G

108227470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113710776-G-C

108227602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113710952-T-C

http://identifiers.org/hco/12/GRCh38#108227613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113710963-C-A

108227745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113711112-A-T

108232905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113712254-T-C

http://identifiers.org/hco/12/GRCh38#108233183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113712638-C-A

108233183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113712638-C-T

108233401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113712837-C-T

http://identifiers.org/hco/12/GRCh38#108233619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113713000-A-C

108233684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113713059-T-C

108233691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113713066-G-A

108234019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113713314-A-T

108234375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113713456-G-T

108234406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113713492-C-G

http://identifiers.org/hco/12/GRCh38#108240235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113715209-C-A

108240235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113715209-C-T

http://identifiers.org/hco/12/GRCh38#108240261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113715235-C-A

http://identifiers.org/hco/12/GRCh38#108240262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113715236-C-A

108240262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113715236-C-G

108240262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113715236-C-T

108240263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113715237-G-A

108240263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113715237-G-C

108240263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113715237-G-T

http://identifiers.org/hco/12/GRCh38#108240408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113715388-C-A

108240408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113715388-C-T

108240519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: synonymous_variant, undefined
orthologous variants: 113715499-T-A

108240519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: synonymous_variant, undefined
orthologous variants: 113715499-T-C

108240519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: synonymous_variant, undefined
orthologous variants: 113715499-T-G

108243831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113716892-C-T

108244326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 113717340-G-A

108244328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 113717342-A-G

108244332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 113717345-T-C

108244425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 113717436-T-C

108244465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 113717477-G-A

108244600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113717570-A-G

108244623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113717593-G-A

108244623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113717593-G-T

108244666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113717639-G-T

108244725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113717698-A-G

http://identifiers.org/hco/12/GRCh38#108244726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113717699-C-A

108244726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113717699-C-G

http://identifiers.org/hco/12/GRCh38#108244727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113717700-C-A

108244727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113717700-C-G

108245698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113717877-T-C

108245899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113718078-G-A

108246336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113718488-C-T

108246337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113718489-C-T

108246508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113718609-C-G

108246508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113718609-C-T

108246512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113718613-A-G

108246539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113718640-C-T

108246540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113718641-A-T

108246846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113718927-G-A

108246895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113718977-C-T

108246930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113719008-C-T

108247019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: intron variant
orthologous variants: 113719095-A-T

http://identifiers.org/hco/12/GRCh38#108248292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113726155-C-A

http://identifiers.org/hco/12/GRCh38#108248645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113726397-C-A

108248645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726397-C-T

http://identifiers.org/hco/12/GRCh38#108248646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113726398-C-A

108248646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726398-C-G

108248824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726528-G-T

108248896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726605-T-A

http://identifiers.org/hco/12/GRCh38#108248988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113726663-C-A

108248988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726663-C-G

108248988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726663-C-T

108249043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726718-A-G

http://identifiers.org/hco/12/GRCh38#108249083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113726766-C-A

108249083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726766-C-T

108249207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726875-G-T

108249220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726892-T-C

http://identifiers.org/hco/12/GRCh38#108249232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113726904-C-A

108249232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726904-C-T

108249258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726934-T-C

108249284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726961-G-T

108249298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726975-G-A

108249298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113726975-G-T

108249339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113727016-A-G

http://identifiers.org/hco/12/GRCh38#108249363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113727040-C-A

http://identifiers.org/hco/12/GRCh38#108249379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113727056-C-A

108249436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113727112-C-T

108249452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113727133-G-T

108249567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113727236-A-G

108249637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113727299-T-C

108249643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113727305-T-C

http://identifiers.org/hco/12/GRCh38#108249690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113727366-C-A

108249690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113727366-C-T

http://identifiers.org/hco/12/GRCh38#108249693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113727369-A-C

108249840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113727501-T-G

108249917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113727581-C-T

108249961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113727626-T-G

108250157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113727816-T-C

108250160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113727819-G-T

108250196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29117
most severe consequence: 3 prime UTR variant
orthologous variants: 113727855-G-A