107702333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42835819-G-A

107702382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42835773-T-C

http://identifiers.org/hco/6/GRCh38#107702592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42835608-A-C

107702651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42835552-T-C

107702651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42835552-T-G

107703430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42835333-C-G

107703652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42835137-G-A

107703652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42835137-G-T

107704323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834564-A-G

http://identifiers.org/hco/6/GRCh38#107704424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42834483-C-A

107704480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834423-A-G

107704487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834416-G-A

107704487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834416-G-T

107704711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834184-T-A

107704722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834173-T-C

107704747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834151-G-A

107704747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834151-G-C

107704747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834151-G-T

107704770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 42834128-T-A

107704770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 42834128-T-C

107704770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 42834128-T-G

107704800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834100-G-A

107704800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834100-G-C

107704800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834100-G-T

107704810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834090-G-A

107704810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834090-G-T

http://identifiers.org/hco/6/GRCh38#107704823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42834077-A-C

107704823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834077-A-G

107704823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834077-A-T

http://identifiers.org/hco/6/GRCh38#107704827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42834073-A-C

107704827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834073-A-G

107704827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834073-A-T

http://identifiers.org/hco/6/GRCh38#107704902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42834013-C-A

107704909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42834006-T-A

107704970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42833951-A-G

107705003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42833916-C-T

107705030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42833890-T-C

107705030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42833890-T-G

107705092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42833828-T-G

107705125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42833796-G-A

107705125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42833796-G-T

107705135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42833786-T-C

107705156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 3 prime UTR variant
orthologous variants: 42833766-T-C

107705249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense variant
orthologous variants: 42833689-G-A

107705263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: synonymous variant
orthologous variants: 42833675-C-T

http://identifiers.org/hco/6/GRCh38#107705348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42833604-A-C

107705350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42833602-G-A

107705350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42833602-G-T

107705414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42833526-G-A

107705414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42833526-G-T

107705425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42833515-A-G

107705441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42833499-G-T

107705448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42833493-A-G

107705498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42833448-A-G

http://identifiers.org/hco/6/GRCh38#107707722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42832149-C-A

107707722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42832149-C-T

107707731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42832140-G-A

107707731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42832140-G-T

http://identifiers.org/hco/6/GRCh38#107707755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42832116-A-C

107707755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42832116-A-G

107707782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42832109-G-A

107707782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42832109-G-C

107707782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42832109-G-T

http://identifiers.org/hco/6/GRCh38#107707795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42832096-C-A

107707846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42832048-C-G

http://identifiers.org/hco/6/GRCh38#107708065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42831831-C-A

107708065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42831831-C-T

http://identifiers.org/hco/6/GRCh38#107708083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42831797-C-A

107708083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42831797-C-T

107708097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42831783-G-A

107708097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42831783-G-T

107708102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42831778-G-T

107708107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42831775-C-T

http://identifiers.org/hco/6/GRCh38#107708117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42831765-C-A

107708181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42831711-T-C

107708364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42831570-G-A

107708395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42831540-G-A

107708603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42831300-G-A

107708638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42831262-T-C

107709188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42829567-A-G

107709188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42829567-A-T

107709220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42829546-A-G

107709323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42829476-T-G

107709334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42829465-C-T

107709371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42829435-T-G

107709383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42829423-G-A

107711645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42828793-T-C

107711717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42828737-A-G

107711717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42828737-A-T

107712012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42828485-C-T

107712030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42828467-A-G

107712046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42828451-G-A

107712087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42828423-C-T

107712100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42828410-G-T

http://identifiers.org/hco/6/GRCh38#107712109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42828400-A-C

107712318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42828192-G-A

107712318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42828192-G-C

http://identifiers.org/hco/6/GRCh38#107712361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42828150-A-C

107712408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42828106-T-A

107712877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42827654-A-G

107712968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42827588-A-G

107712969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42827587-T-A

107713119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42827423-C-T

http://identifiers.org/hco/6/GRCh38#107713313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42827228-C-A

107714099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42826966-G-A

107714125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42826940-C-T

107714348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42826684-A-G

107714358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42826665-C-G

107714415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42826580-G-A

http://identifiers.org/hco/6/GRCh38#107714498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42826454-A-C

107714657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42826248-C-T

107714817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42826124-A-G

107714851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42826093-C-T

107714857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42826087-G-A

107715411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825836-T-C

107715486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825769-T-C

107715516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825739-T-C

107715555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825718-T-C

107715618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825660-A-G

107715696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825595-G-C

107715719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825582-G-T

107715732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825569-G-A

107715773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825530-G-A

107715780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825523-A-G

http://identifiers.org/hco/6/GRCh38#107715799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42825493-C-A

107715799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825493-C-T

107715923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825365-G-A

107715932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825348-G-T

107715973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825307-T-A

107716010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825250-G-T

107716024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825236-G-A

107716079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825195-C-G

http://identifiers.org/hco/6/GRCh38#107716137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42825147-A-C

107716145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825139-T-C

107716149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825135-G-C

107716218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825096-G-A

107716292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42825011-C-T

107716392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42824917-T-G

107716614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42824522-G-A

107716664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42824412-G-A

107716815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42824271-C-T

http://identifiers.org/hco/6/GRCh38#107719702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42823985-C-A

107719752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823948-A-G

107719752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823948-A-T

107719778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823922-G-A

107719778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823922-G-T

107719805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823890-A-G

http://identifiers.org/hco/6/GRCh38#107719943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42823678-C-A

107719943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823678-C-G

107719948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823673-T-C

107719964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823664-T-C

107720065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823582-T-C

http://identifiers.org/hco/6/GRCh38#107720145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42823567-C-A

107720170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823556-C-G

107720170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823556-C-T

107720191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823542-G-T

107720227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823521-G-T

107720228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823520-A-T

http://identifiers.org/hco/6/GRCh38#107720312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42823464-C-A

http://identifiers.org/hco/6/GRCh38#107720351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42823425-C-A

107720351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823425-C-T

107720360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823416-A-G

107720493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823305-G-C

107720493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823305-G-T

http://identifiers.org/hco/6/GRCh38#107720498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42823300-A-C

http://identifiers.org/hco/6/GRCh38#107720521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42823274-C-A

107720545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823251-G-A

107720545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823251-G-T

http://identifiers.org/hco/6/GRCh38#107720570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42823228-C-A

107720570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823228-C-G

107720571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823227-T-C

http://identifiers.org/hco/6/GRCh38#107720602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42823196-A-C

107720602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823196-A-G

http://identifiers.org/hco/6/GRCh38#107720619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42823181-C-A

107720619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823181-C-G

107720619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823181-C-T

http://identifiers.org/hco/6/GRCh38#107720622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42823178-C-A

107720622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823178-C-G

107720622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42823178-C-T

107720819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42823019-G-A

http://identifiers.org/hco/6/GRCh38#107720834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42823004-C-A

107720834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42823004-C-T

107720840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42822998-A-T

107720956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42822900-A-G

107720958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42822898-G-A

107720958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42822898-G-C

http://identifiers.org/hco/6/GRCh38#107721020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42822838-C-A

107721020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822838-C-T

107721021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822837-A-G

107721099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822765-T-G

107721104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822760-G-A

107721104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822760-G-C

107721104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822760-G-T

http://identifiers.org/hco/6/GRCh38#107721111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42822751-C-A

107721111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822751-C-G

107721111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822751-C-T

107721116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822746-A-G

107721119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822743-A-G

107721119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822743-A-T

http://identifiers.org/hco/6/GRCh38#107721133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42822730-C-A

107721133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822730-C-T

107721225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822655-C-T

107722316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822591-C-T

107722337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822567-G-A

http://identifiers.org/hco/6/GRCh38#107722533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42822399-C-A

http://identifiers.org/hco/6/GRCh38#107722538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42822378-A-C

107722623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822343-G-C

107722654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822312-T-C

107722656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822310-G-A

107722927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42821811-A-G

107722934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42821804-T-C

107723081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42821697-T-A

107723081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42821697-T-C

http://identifiers.org/hco/6/GRCh38#107723139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42821651-C-A

107723585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42821228-A-G

107723613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42821208-A-G

107723630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42821186-A-G

107723821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42821007-G-C

107723931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42820894-C-T

107723943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42820882-T-C

107724040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42820806-T-C

http://identifiers.org/hco/6/GRCh38#107724069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42820775-A-C

107724209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42820672-A-G

107724498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42820430-A-G

107724654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42820278-C-G

107724810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42820116-A-T

107729733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42818783-A-G

http://identifiers.org/hco/6/GRCh38#107729943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42818362-C-A

http://identifiers.org/hco/6/GRCh38#107729981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42818324-C-A

107729981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42818324-C-T

107730052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42818266-T-C

107730126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42818191-G-A

107730273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42818069-G-C

107730592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817808-T-C

107730765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817593-T-C

107730952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817486-T-C

http://identifiers.org/hco/6/GRCh38#107731104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42817384-A-C

107731389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817125-A-G

107731389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817125-A-T

107731502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816973-G-A

107731502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816973-G-T

107731721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816802-G-A

107731785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816746-G-A

107731807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816717-C-T

107731851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816674-A-G

107731851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816674-A-T

107731853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816672-A-G

107731856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816666-A-G

107731878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816643-G-T

http://identifiers.org/hco/6/GRCh38#107731929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42816603-C-A

107731929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816603-C-T

107731946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816594-G-T

107732016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42816529-T-C

107732076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42816484-T-C

107732084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42816477-G-T

107732091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42816471-T-C

http://identifiers.org/hco/6/GRCh38#107732158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42816427-C-A

107732158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42816427-C-T

107732280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42816300-A-G

107732285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42816295-G-T

107732549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816036-C-T

107732656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42815932-G-T

107732840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42815757-A-T

107743228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42812312-C-T

107743337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42812201-T-G

107743600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42811977-C-T

107744715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42811325-C-T

107744733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42811307-G-A

107744759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42811281-G-A

107744841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42811218-A-T

107744858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42811205-G-T

107744914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42811154-G-A

107744914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42811154-G-T

107744993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42811097-G-A

107745068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42811022-A-G

107745128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42810962-T-G

http://identifiers.org/hco/6/GRCh38#107745153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42810939-C-A

107745180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42810912-A-G

107745180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42810912-A-T

http://identifiers.org/hco/6/GRCh38#107745191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42810901-C-A

http://identifiers.org/hco/6/GRCh38#107745282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42810836-C-A

http://identifiers.org/hco/6/GRCh38#107745377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42810747-C-A

http://identifiers.org/hco/6/GRCh38#107745396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42810728-A-C

107745396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42810728-A-G

107745403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42810721-T-C

107745408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42810716-G-T

107745437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42810678-G-T

107746184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806973-G-T

107746198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806959-G-T

107746234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806925-G-T

107746238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806921-T-A

107746238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806921-T-C

107746253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806910-A-T

107746254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806909-T-C

107746254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806909-T-G

107746288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806896-G-T

107746297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806887-T-C

107746407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806835-T-C

http://identifiers.org/hco/6/GRCh38#107746487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42806773-C-A

107746513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806747-A-G

http://identifiers.org/hco/6/GRCh38#107746556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42806715-C-A

107746556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806715-C-T

107746598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806673-G-A

107746598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42806673-G-T

107746703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42806584-C-T

107746738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42806549-C-G

107746738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42806549-C-T

107746840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42806447-C-T

107746850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42806437-T-C

http://identifiers.org/hco/6/GRCh38#107746856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42806431-C-A

107746856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42806431-C-G

107746856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42806431-C-T

http://identifiers.org/hco/6/GRCh38#107746857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42806430-C-A

107746857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42806430-C-T

http://identifiers.org/hco/6/GRCh38#107746923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42806362-C-A

107746923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42806362-C-T

107746926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42806359-G-T

http://identifiers.org/hco/6/GRCh38#107746931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42806354-C-A

107746931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42806354-C-T

107746941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42806344-G-T

http://identifiers.org/hco/6/GRCh38#107746946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42806339-C-A

107746946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42806339-C-T

107747016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42806304-G-A

107747016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42806304-G-T

http://identifiers.org/hco/6/GRCh38#107747031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42806289-A-C

http://identifiers.org/hco/6/GRCh38#107747038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42806282-C-A

107747042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42806279-C-T

107747047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42806274-G-C

107747113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42806208-T-C

107747368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42805977-C-T

107748042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42802015-T-A

107748076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42801989-C-T

107748189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42801875-T-A

107748238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42801826-T-C

http://identifiers.org/hco/6/GRCh38#107748312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42801770-A-C

107748312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42801770-A-G

107748903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42801379-T-A

107748938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42801344-C-G

107749119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42801173-T-C

http://identifiers.org/hco/6/GRCh38#107749123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42801169-C-A

107749123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42801169-C-T

107749126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42801166-G-T

107749138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42801154-A-G

107749256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 42801046-T-C

http://identifiers.org/hco/6/GRCh38#107749582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42800278-C-A

107749625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42800236-G-T

107749630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42800230-C-T

http://identifiers.org/hco/6/GRCh38#107749634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42800226-C-A

107749634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42800226-C-T

107749824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42800035-G-C

107749841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42800018-G-A

http://identifiers.org/hco/6/GRCh38#107749957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42799909-C-A

107749957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42799909-C-T

107750061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42799808-T-C

107750107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42799756-G-A

107750205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42799665-A-G

107750330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42799570-G-C

107750358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42799546-A-G

107750388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42799516-T-C

http://identifiers.org/hco/6/GRCh38#107750392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42799513-C-A

107750392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42799513-C-T

107750438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42799467-G-A

107750731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42799181-A-T

107753390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42797407-G-A

107753481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42797315-G-A

107753768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42796924-T-C

107753949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42796809-G-A

107753960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42796798-A-G

107754008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42796755-G-A

107754226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42796565-T-C

107754388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42796414-A-G

107754507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42796320-G-A

107754609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42796223-G-A

107754687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42796140-A-G

107754690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42796137-C-G

107769091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42791744-C-T

107769124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42791716-G-A

107769124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42791716-G-C

107769428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42791437-T-C

107770086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42790681-C-G

107770173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42790609-T-G

http://identifiers.org/hco/6/GRCh38#107770582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42790252-A-C

107771445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42788963-C-T

107771469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42788940-G-A

107771491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42788918-T-G

http://identifiers.org/hco/6/GRCh38#107771740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42788680-A-C

107771740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42788680-A-G

107771760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42788660-A-G

107771981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42788419-C-G

107771981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42788419-C-T

http://identifiers.org/hco/6/GRCh38#107772079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42788316-C-A

http://identifiers.org/hco/6/GRCh38#107772084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42788311-C-A

http://identifiers.org/hco/6/GRCh38#107772123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42788273-C-A

http://identifiers.org/hco/6/GRCh38#107772135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42788261-C-A

107772135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42788261-C-T

http://identifiers.org/hco/6/GRCh38#107772137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42788259-A-C

107772137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42788259-A-G

107772138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42788258-T-C

107772165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42788232-G-A

107772215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42788182-G-T

107772235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42788162-A-G

107772391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42788006-G-C

107772391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42788006-G-T

107772395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42788002-T-A

107772433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42787964-G-A

107772433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42787964-G-T

http://identifiers.org/hco/6/GRCh38#107772504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42787900-A-C

107772772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42787536-C-T

107773115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42787224-G-A

http://identifiers.org/hco/6/GRCh38#107773258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42787085-C-A

107773355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42786968-G-T

107773400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42786906-T-G

107773456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42786851-G-A

107773456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42786851-G-T

107774152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42786212-A-G

107774335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42786025-G-A

107774336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42786024-A-G

107774488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42785887-A-G

107774570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42785815-C-G

107774585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42785800-T-G

http://identifiers.org/hco/6/GRCh38#107777588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42781757-A-C

107779677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42780736-T-C

107779709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42780704-G-A

107779752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42780669-G-C

107780030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42780398-G-A

107780162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42780196-C-G

107780162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42780196-C-T

107780211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42780078-C-T

107781693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42779306-G-A

107782005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42779029-A-G

107782230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42778821-T-C

107783721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42778132-C-T

http://identifiers.org/hco/6/GRCh38#107783730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42778118-A-C

107783781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42778060-T-C

107784214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42777739-C-T

http://identifiers.org/hco/6/GRCh38#107784270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42777676-C-A

107784304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42777643-G-A

107784344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42777619-A-T

107784429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42777550-G-T

107786338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42775535-G-A

http://identifiers.org/hco/6/GRCh38#107786422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42775439-C-A

107786422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42775439-C-G

107786422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42775439-C-T

107786449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42775412-G-C

107786481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42775380-G-T

107786517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42775350-C-T

http://identifiers.org/hco/6/GRCh38#107786853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42774343-A-C

107787259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42773999-A-G

107787633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42773607-C-G

107787760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42773495-A-G

107788367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42772467-C-T

107788888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42771996-G-A

http://identifiers.org/hco/6/GRCh38#107788919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42771978-C-A

107788919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42771978-C-G

107789275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42771650-A-T

107789655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42770949-C-T

107789735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42770905-T-C

http://identifiers.org/hco/6/GRCh38#107789741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42770899-A-C

107789801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42770848-C-T

107790002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42770670-T-A

107790470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42770386-C-T

107790501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42770360-T-C

107790581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42770300-A-G

107792064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42769289-C-T

107792160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42769191-C-T

107792162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42769189-G-A

107792162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42769189-G-C

107792174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42769176-C-T

107792809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42768639-T-C

107794199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42767161-G-T

107794364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42767005-A-G

107794643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42766746-A-G

107794891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42766434-A-G

107795072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42766266-C-T

107795386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42765901-T-G

107795401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42765870-A-G

107795413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42765857-C-T

http://identifiers.org/hco/6/GRCh38#107795856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42765636-A-C

http://identifiers.org/hco/6/GRCh38#107795859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42765633-C-A

107795871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42765621-A-G

107796072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42765456-C-T

107796163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42765367-T-A

107796306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42765241-T-C

107796436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42765115-T-C

107797068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42764208-A-G

107797075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42764202-T-C

107797465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42763778-A-G

107801239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42755383-C-G

107801317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42755337-T-C

107801387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42755269-G-A

107801572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42755067-T-C

107805742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42750972-C-G

107805742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42750972-C-T

107806011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42750712-C-T

107806084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42750653-C-T

107806158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42750349-C-T

107806175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42750333-A-G

107806598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42749521-T-C

107806644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42749474-T-C

107806662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42749456-A-G

107806711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42749406-C-T

107806729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42749395-A-G

107806942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42749235-C-T

107806983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42749195-G-A

107807001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42749188-G-A

107807109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42749092-G-T

107807184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42749019-G-A

107807184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42749019-G-C

107807405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42748803-C-T

107807491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42748719-G-A

http://identifiers.org/hco/6/GRCh38#107807521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42748689-C-A

107807700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42748525-C-T

107807825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42748404-A-G

107807839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42748390-T-A

107807871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42748358-T-C

107807877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42748352-G-T

107808069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42748189-G-A

107809540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42746919-A-G

107809695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42746771-A-G

107809835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42746643-C-G

107809835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42746643-C-T

107809845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42746637-C-G

107809940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42746612-T-G

107810227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42746395-C-G

107810255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42746360-G-T

107810307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42746293-T-C

107810439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42746020-G-A

107816979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42743160-G-C

107817277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42742857-T-C

107817675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42742252-A-G

107817675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42742252-A-T

107817805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42742125-T-G

107818815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42741477-C-T

107818882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42741412-G-A

107818931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42741365-G-C

107819448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42740916-C-T

http://identifiers.org/hco/6/GRCh38#107819622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42740775-C-A

107819693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42740717-T-A

107819758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42740643-A-T

107820046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42740375-T-C

http://identifiers.org/hco/6/GRCh38#107820519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42740140-C-A

107820551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42740096-C-T

107820663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42739980-G-A

107820663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42739980-G-C

107821730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42739090-T-C

107822010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42738881-A-T

107822179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42738697-T-C

107822193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42738683-T-C

107822985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42737994-G-T

107823030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42737932-G-A

http://identifiers.org/hco/6/GRCh38#107823041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42737922-C-A

http://identifiers.org/hco/6/GRCh38#107823326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42737643-C-A

107823910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42737072-G-A

107823919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42737063-T-C

107823954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42737026-A-G

http://identifiers.org/hco/6/GRCh38#107824214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#42736756-A-C

107824280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42736685-C-T

107824460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21397
most severe consequence: intron variant
orthologous variants: 42736501-C-T