http://identifiers.org/hco/7/GRCh38#89989435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6043510-C-A

89989491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6043467-T-C

http://identifiers.org/hco/7/GRCh38#89989667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6043315-A-C

89989672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6043310-G-T

89989683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6043298-G-A

89989683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6043298-G-C

89989757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6043220-T-C

89989792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6043185-T-C

http://identifiers.org/hco/7/GRCh38#89989923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6043066-C-A

89989939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6043050-G-A

89989975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6043016-C-T

89990914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6042961-C-T

89990984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6042892-A-G

89991114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6042763-A-G

http://identifiers.org/hco/7/GRCh38#89991144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6042732-C-A

89991144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6042732-C-G

89991191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6042685-G-A

89991259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6042639-G-A

89991342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6042552-G-A

89993116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6041261-G-A

89993174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6041181-A-T

89993268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6041087-C-T

89993269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6041086-A-G

89993662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6040742-G-A

89995016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6040000-T-C

http://identifiers.org/hco/7/GRCh38#89995052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6038635-C-A

89995052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6038635-C-T

89995114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6038574-G-A

http://identifiers.org/hco/7/GRCh38#89995140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6038548-C-A

89995140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6038548-C-T

89998378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6037218-T-C

89998634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6036931-A-G

89998696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6036867-G-A

89998936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6036632-G-A

89998936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6036632-G-T

89999088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6036458-G-A

89999088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6036458-G-C

http://identifiers.org/hco/7/GRCh38#89999346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6036192-C-A

89999346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6036192-C-T

89999712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6035885-G-T

90000051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6035525-A-G

90000108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6035410-A-G

90000619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6034946-C-G

http://identifiers.org/hco/7/GRCh38#90000827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6034765-C-A

90000827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6034765-C-T

90003124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6032002-T-C

90003138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6031988-G-C

90003164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6031964-G-T

90003229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6031905-C-T

90003296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6031829-T-C

90003888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6026711-C-G

90004040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6026574-T-C

http://identifiers.org/hco/7/GRCh38#90004106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6026514-C-A

90004106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6026514-C-T

90004431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6026189-G-A

http://identifiers.org/hco/7/GRCh38#90005789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6024006-C-A

90005826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6023969-A-T

90005869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6023928-A-T

90005870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6023927-T-A

90006217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6023554-A-T

90006234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

90006568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6023218-C-T

90006680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6023107-A-G

90006690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6023096-G-T

90006955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6022825-C-T

90007860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6021972-T-C

90008060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6021771-A-G

90008382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6021462-C-T

90008455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6021389-A-G

90008828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6021018-A-G

90009749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6016645-T-C

90009996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6016375-T-C

90010144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6016220-C-T

90010277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6016095-T-C

90010358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6016012-T-C

90011557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6015228-G-C

90011681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6015094-C-T

90011713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6015068-G-A

90011757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6014998-T-A

90011776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6014979-T-G

90016440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6012284-G-T

90016566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6012157-T-C

90016871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6011856-A-G

90017525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6011202-C-T

90017759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6010983-G-C

90017968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6010225-C-G

90017968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6010225-C-T

90018114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6010078-G-C

90018700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6009511-T-C

90019407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6008057-C-T

http://identifiers.org/hco/7/GRCh38#90019457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6008008-C-A

90019466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6007889-G-A

90019628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6007730-A-G

90019664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6007694-G-A

90021973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6005807-G-C

90022043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6005738-G-T

90022253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6005390-G-A

90022262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6005381-C-T

90022383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6005268-A-G

90032049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6001034-A-G

http://identifiers.org/hco/7/GRCh38#90032100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6000981-A-C

90032100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6000981-A-G

90032405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6000689-T-C

90032587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6000515-A-G

http://identifiers.org/hco/7/GRCh38#90032593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#6000509-A-C

90033530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5998084-T-C

90033683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5997951-T-C

90033877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5997829-G-A

90033886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5997820-G-A

90034225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5997511-T-C

90034325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5997350-C-T

http://identifiers.org/hco/7/GRCh38#90034405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5997281-C-A

90034405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5997281-C-T

90034760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5996916-C-G

90034760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5996916-C-T

90034788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5996888-T-A

90034804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5996872-C-G

90034866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5996805-T-C

90035022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5996555-C-T

90035119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5996394-A-G

90035151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5996362-G-T

90035300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5996208-T-A

90035356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5996153-C-T

90037615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5993989-C-T

90037616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5993988-G-A

90037650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5993964-A-G

90037658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5993956-G-T

http://identifiers.org/hco/7/GRCh38#90037962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5993684-C-A

90038009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5993637-T-G

90038139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5993512-A-T

90038239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5993413-C-T

90038261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5993392-G-A

90038679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5993028-G-C

90039103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5992510-C-T

90039220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5992379-A-G

90039625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5991933-C-T

90039657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5991902-G-A

90039658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5991901-G-A

90039964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5991647-C-T

90040028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5991594-T-C

90040222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5991039-T-C

90040222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5991039-T-G

90040525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5983040-G-A

90040567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5983010-C-G

90050951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5981486-C-G

90050951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5981486-C-T

90051039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5981403-T-G

90051048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5981394-T-C

90051217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5981240-C-G

90051217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5981240-C-T

90051327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5981128-T-C

90051537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5980933-T-C

90051618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5980855-A-G

90051693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5980784-T-C

90051741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5980745-G-C

90051787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5980699-C-T

90051906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5980563-T-G

90051983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5980487-G-A

90052068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5980424-C-T

90052359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5980182-G-T

90052376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5980165-C-T

90052476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5980065-G-C

90052522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5980025-A-G

http://identifiers.org/hco/7/GRCh38#90055271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5978177-A-C

90055440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5978034-T-C

90055440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5978034-T-G

90057214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5976915-G-A

90057223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5976906-C-T

90057235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5976901-A-G

90057276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5976860-A-G

http://identifiers.org/hco/7/GRCh38#90057657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5976556-A-C

90057741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5976490-C-T

90057762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5976469-C-G

90057998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5976266-T-C

90057998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5976266-T-G

90058048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5976216-G-A

90058354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5975899-G-C

90058415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5975838-T-G

90059147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5975022-A-T

90059357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5974838-C-T

90059497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5974487-G-A

http://identifiers.org/hco/7/GRCh38#90059500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5974484-C-A

90060045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5973786-G-A

90060045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5973786-G-C

90060355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5973476-G-A

90060604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5973235-T-A

90060885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5973003-T-C

90061025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5972881-C-T

90061044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5972863-G-C

90061180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5972745-T-C

90061524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5972082-A-G

90061559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5972022-G-A

http://identifiers.org/hco/7/GRCh38#90061699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5971904-C-A

90061994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5971619-C-T

90062031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5971580-T-C

90062291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5971327-G-A

90062329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5971289-A-G

http://identifiers.org/hco/7/GRCh38#90062331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5971287-C-A

90062382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5971236-C-T

90062400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5971219-T-C

90062462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5971151-G-A

90062462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5971151-G-T

90062804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5970836-C-T

90064266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5970617-G-A

90064441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5970473-G-A

http://identifiers.org/hco/7/GRCh38#90064516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5970416-A-C

90064584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5970351-G-A

90065768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5970328-T-C

http://identifiers.org/hco/7/GRCh38#90065796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5970300-A-C

http://identifiers.org/hco/7/GRCh38#90065862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5970229-C-A

90066272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5969860-T-C

90066351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5969788-C-T

90066413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5969723-A-G

90066435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5969701-G-C

90066677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5969533-C-T

90067351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5967716-C-G

90067451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5967614-C-T

90067492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5967574-C-G

http://identifiers.org/hco/7/GRCh38#90067504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5967562-C-A

90067504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5967562-C-G

90067532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5967537-G-T

90067715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5967376-A-G

http://identifiers.org/hco/7/GRCh38#90067908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5967180-A-C

90068036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5966947-T-C

90068072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5966909-T-C

90068098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5966879-G-C

90068109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5966868-A-G

90068170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5966826-T-C

90068184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5966817-T-C

90068185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5966816-G-A

90068201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5966801-G-A

90068297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5966707-G-A

90068297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5966707-G-T

http://identifiers.org/hco/7/GRCh38#90068559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5966478-A-C

90068559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5966478-A-G

90068559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5966478-A-T

http://identifiers.org/hco/7/GRCh38#90068596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5966448-A-C

90069874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5963503-T-C

90070107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5963274-G-C

90070107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5963274-G-T

90070116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5963265-C-G

90070116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5963265-C-T

http://identifiers.org/hco/7/GRCh38#90077423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5962717-A-C

90077513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5962630-T-C

http://identifiers.org/hco/7/GRCh38#90077676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5962476-A-C

90077701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5962451-A-G

90077773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5962385-G-T

90077851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5962316-T-G

http://identifiers.org/hco/7/GRCh38#90078161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5961787-C-A

90078278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5961674-A-G

90080821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5950831-T-C

90081048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5950478-T-A

http://identifiers.org/hco/7/GRCh38#90081770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5949573-C-A

90081901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5949438-T-C

90082163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5949166-G-T

90082574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5948104-T-C

90082586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5948092-A-G

90082686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5947993-T-C

http://identifiers.org/hco/7/GRCh38#90082729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5947949-A-C

90082822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5947897-G-A

90082871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5947863-A-G

90082871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5947863-A-T

http://identifiers.org/hco/7/GRCh38#90082874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5947860-A-C

http://identifiers.org/hco/7/GRCh38#90083019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5947731-C-A

90083019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5947731-C-G

90083114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5947625-T-C

90083234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5947504-G-A

90083235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5947503-G-A

90083428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5947313-G-A

90083428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5947313-G-T

90083671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5947131-G-A

90083953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5945426-A-G

90084179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5945204-G-A

90084185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5945198-G-A

90084328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5945043-A-G

90084407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5944964-G-C

90085049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5944309-C-G

90085198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5944173-T-C

90085783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5943931-G-C

90085783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5943931-G-T

90085916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5943810-T-C

90085929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5943800-G-A

90086564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5942397-C-T

90086565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5942396-A-G

90093919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5929619-T-G

90093984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5929564-T-C

90093984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5929564-T-G

90094341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5929205-G-A

90094643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5928895-T-C

90095121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5928592-T-C

90095423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5928325-T-C

90095436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5928305-A-G

90095794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5928003-G-A

90095798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5927999-G-C

90096266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5927188-T-A

90096380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5927104-A-G

90096401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5927088-G-A

90096522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5926963-C-T

90096702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5926779-A-G

90097024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5926449-C-G

90098119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5926071-A-G

90098299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5925898-T-C

90098991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5924188-G-A

90099002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5924177-A-G

90100790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5921791-G-A

90101336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5921557-C-G

90101865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5921018-G-A

90102139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5920772-A-G

90102139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5920772-A-T

90102231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5920721-T-C

http://identifiers.org/hco/7/GRCh38#90102938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5919752-C-A

90103248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5918448-T-C

90103474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5918217-C-G

90103499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5918193-T-C

90103565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5918126-G-T

90103763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5917920-T-C

90103791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5917886-T-A

90151664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5800796-A-T

90151668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5800795-T-C

90152856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5800111-T-A

http://identifiers.org/hco/7/GRCh38#90154438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5799339-C-A

90154438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5799339-C-T

90154467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5799316-T-C

90154527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5799248-G-A

90154527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5799248-G-T

http://identifiers.org/hco/7/GRCh38#90154581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5799209-C-A

90154581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5799209-C-G

90154581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5799209-C-T

90154584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5799206-G-A

90154584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5799206-G-T

90154615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5799188-C-T

90154647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5799156-G-T

90154654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5799149-A-G

90154803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5799060-T-C

90154803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5799060-T-G

90155101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5798796-G-A

90155108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5798789-T-C

http://identifiers.org/hco/7/GRCh38#90155389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5798517-A-C

90155454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5798449-C-T

90155666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5798247-T-C

90155734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5798198-G-C

90155898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5798033-T-C

90155960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5797974-A-G

90155980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5797954-T-C

90156077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5797864-C-T

90157101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5797549-A-G

90158945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5794012-T-C

90159145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5793815-G-T

90159183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5793776-C-T

90159209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5793750-C-T

http://identifiers.org/hco/7/GRCh38#90159629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5793227-C-A

90159629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5793227-C-G

90159629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5793227-C-T

90159750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5792946-T-C

http://identifiers.org/hco/7/GRCh38#90159768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5792928-C-A

90159768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5792928-C-T

90159801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5792895-A-G

90159820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5792876-A-G

http://identifiers.org/hco/7/GRCh38#90159891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5792811-C-A

90159891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5792811-C-T

90159912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5792790-A-G

90159912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5792790-A-T

90159916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5792786-T-C

90159926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5792776-T-C

90159959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5792746-A-G

http://identifiers.org/hco/7/GRCh38#90160299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5792455-A-C

90160532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5792280-T-G

http://identifiers.org/hco/7/GRCh38#90160721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5790927-A-C

90160721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5790927-A-G

http://identifiers.org/hco/7/GRCh38#90160862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5790803-C-A

90160862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5790803-C-T

90160863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5790802-A-G

90160880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5790785-G-C

90160976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5790689-T-C

90161261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5790404-T-A

90161340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5790332-G-C

90161399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5790265-T-C

90161572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5790117-T-C

90161587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5790104-C-T

90161629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5790055-T-C

http://identifiers.org/hco/7/GRCh38#90161638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5790046-A-C

90162041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5789831-G-A

90162041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5789831-G-C

90162124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5789764-T-G

http://identifiers.org/hco/7/GRCh38#90162204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5789691-C-A

90162204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5789691-C-G

http://identifiers.org/hco/7/GRCh38#90162290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5789597-A-C

90162290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5789597-A-T

90162774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5789443-C-T

http://identifiers.org/hco/7/GRCh38#90162838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5789379-A-C

http://identifiers.org/hco/7/GRCh38#90162914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5788950-A-C

90162914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788950-A-G

90162933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788931-A-G

http://identifiers.org/hco/7/GRCh38#90162935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5788928-A-C

90162935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788928-A-G

http://identifiers.org/hco/7/GRCh38#90162936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5788927-A-C

90162936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788927-A-G

90162936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788927-A-T

90162945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788918-A-G

90162945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788918-A-T

90163059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788820-G-A

90163081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788777-T-A

90163081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788777-T-C

90163087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788771-G-T

90163171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788687-G-A

90163184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788673-T-C

90163658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788329-G-A

90163739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788250-T-C

90163783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5788204-A-G

90163936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5787292-T-C

90164124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5787122-G-C

90164579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5786569-C-G

http://identifiers.org/hco/7/GRCh38#90164822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5786330-C-A

90165347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5785105-A-G

90165864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5784648-A-G

90165920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5784595-C-T

90165989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5784538-G-T

90166353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783392-T-C

90166652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783137-G-A

90178198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5773120-A-G

90178291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5773014-T-C

90178449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5772862-G-A

90179197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5772205-T-C

90179227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5772167-A-G

http://identifiers.org/hco/7/GRCh38#90179496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5771720-A-C

90179497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771719-C-T

90179644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771604-T-C

90179796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771485-A-G

90180324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5770972-C-T

http://identifiers.org/hco/7/GRCh38#90180580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5770731-A-C

90180793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5770517-G-A

90181198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5770116-T-G

90181254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5770027-A-T

90181497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5769822-G-A

90181929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5769625-T-A

90181931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5769623-T-A

90181933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5769621-T-A

90181935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5769619-A-T

90181937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5769617-A-T

90181945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5769609-A-T

http://identifiers.org/hco/7/GRCh38#90181967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5769587-C-A

90182246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5768824-G-C

90182321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5768747-T-A

90182647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5768412-T-C

90182837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5768363-T-A

90182837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5768363-T-G

90183208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5768161-G-T

90183314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5768053-C-T

90183470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5767917-T-C

90183509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5767872-T-C

90183573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5767821-T-C

90183656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5767731-G-T

90183849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766880-C-G

90183980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766753-A-G

90184203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766596-C-T

90184274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766524-C-G

90184455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766356-T-C

90184585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766228-T-G

90184603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766210-G-C

90184738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766090-C-G

http://identifiers.org/hco/7/GRCh38#90184895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5765970-A-C

http://identifiers.org/hco/7/GRCh38#90186607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5764479-A-C

90186729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5764339-T-C

90186769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5764299-G-A

http://identifiers.org/hco/7/GRCh38#90186794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5764275-A-C

http://identifiers.org/hco/7/GRCh38#90186898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5764147-C-A

90186898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5764147-C-G

90186966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5764088-A-G

90187100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5763979-A-T

90187165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5763930-T-A

http://identifiers.org/hco/7/GRCh38#90187168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5763927-A-C

90187170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5763925-T-C

http://identifiers.org/hco/7/GRCh38#90187212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5763881-A-C

http://identifiers.org/hco/7/GRCh38#90199695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5759664-A-C

90200187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5759010-C-G

90200296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5758799-A-T

90200412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5758690-T-A

90200520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5758531-G-A

90200520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5758531-G-C

90201882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5756425-T-G

90207383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5748542-A-G

90207435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5748499-C-T

90207709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5748074-T-A

90207709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5748074-T-G

90207774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5748005-G-A

90207792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5747987-C-T

90209244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5746634-G-T

90209714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5745886-A-T

90209747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5745857-T-C

90209860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5745747-G-T

90209885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5745722-A-G

http://identifiers.org/hco/7/GRCh38#90209927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#5745676-C-A

90209927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5745676-C-T

90209955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5745648-A-G

90209987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5745629-G-T

90210532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5745108-G-A

90210587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5745056-T-C

90210587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5745056-T-G

90210607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5745033-G-C

90210949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5744707-T-C

90211162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5744511-T-C

90211209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5744454-G-A

90211317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5744387-T-C

90211374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5744344-G-A

90211374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5744344-G-T

http://identifiers.org/hco/7/GRCh38#90211475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40820
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#5744252-C-A