16189591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36620830-G-A

16189773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36620652-T-C

16189801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36620639-A-G

http://identifiers.org/hco/7/GRCh38#16189840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36620600-C-A

16189971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36620469-A-G

16190008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36620433-T-C

16190008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36620433-T-G

16190489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36619674-C-T

16193354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36618979-A-G

16193385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36618943-T-G

16193629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36618698-T-C

16194505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36618336-C-G

http://identifiers.org/hco/7/GRCh38#16194701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36618143-C-A

16195020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617811-A-G

16195087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617745-T-A

16195087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617745-T-C

http://identifiers.org/hco/7/GRCh38#16195106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36617726-C-A

http://identifiers.org/hco/7/GRCh38#16195115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36617717-A-C

16195115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617717-A-G

http://identifiers.org/hco/7/GRCh38#16195116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36617716-A-C

http://identifiers.org/hco/7/GRCh38#16195236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36617616-A-C

16195236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617616-A-G

16195538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617329-C-G

16195586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617287-T-C

16195747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617151-T-C

16195822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36617076-A-G

16196356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616984-C-T

16196399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616947-T-A

http://identifiers.org/hco/7/GRCh38#16196400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36616946-A-C

http://identifiers.org/hco/7/GRCh38#16196429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36616933-C-A

16196589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616776-G-A

16196712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616694-A-G

16196782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616606-G-A

16196902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616503-T-C

16196986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616407-T-C

16197018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616182-T-A

16197023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36616177-A-G

16197319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36615849-C-T

16200369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36614867-T-A

16200370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36614866-C-T

16200425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36614807-T-C

16200461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36614771-T-A

16200461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36614771-T-C

16200542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36614684-G-T

16200702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36614493-G-C

16201211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613926-T-A

16201211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613926-T-C

16201796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613892-C-T

16201968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613691-T-G

16202120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613513-T-G

16202152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613482-T-C

16202237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613440-T-C

16202254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613423-A-G

16202731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36612994-G-C

16202998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36612710-T-G

16203018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36612690-T-C

http://identifiers.org/hco/7/GRCh38#16203173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36612548-A-C

16203175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36612546-T-C

16203216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36612504-C-T

16203254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36612482-C-T

16205454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611181-C-T

16205544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611091-A-G

http://identifiers.org/hco/7/GRCh38#16205573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36611062-C-A

16205667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610959-G-C

16205802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610828-A-G

16205836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610794-T-C

16205969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610665-T-A

16206177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610475-C-T

http://identifiers.org/hco/7/GRCh38#16206815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36608914-A-C

16206871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36608858-C-T

http://identifiers.org/hco/7/GRCh38#16207002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36608725-C-A

16207017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36608712-T-C

16207017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36608712-T-G

16207207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36608033-T-C

16207303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36607939-G-T

16207330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36607929-T-C

16207488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36607812-T-C

16207696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36607591-T-C

16207891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36607414-A-G

16208075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36607260-C-T

16208164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36607174-T-C

16208165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36607173-G-A

16208358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36607037-A-G

16208406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36606982-T-C

16209957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

16210017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

16210062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

16210088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

16210154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

16211180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604400-C-T

16211988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603099-T-C

16212017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603070-A-G

16212018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603069-G-A

16212018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603069-G-T

16212084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603010-C-T

16212110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602981-T-G

16212832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36601938-G-A

16214876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36600649-A-G

16214998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36600538-T-A

16214998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36600538-T-C

16215298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36599890-T-C

16215701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36599524-G-T

16215807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36599450-G-C

16215948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598073-T-G

http://identifiers.org/hco/7/GRCh38#16215959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36598062-C-A

16215959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598062-C-T

16215973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598048-A-G

16216127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36597896-A-G

16216166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36597857-G-A

16216166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36597857-G-T

16216167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36597856-G-A

16216167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36597856-G-T

16216181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36597842-A-G

16216343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36597704-A-G

http://identifiers.org/hco/7/GRCh38#16216354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36597687-A-C

16216354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36597687-A-T

16224213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36595429-T-C

16225016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36594585-T-C

16225036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36594566-A-G

16225065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36594537-T-C

16225172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36594390-A-G

16225205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36594353-A-G

16225531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36593542-A-T

16225644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36593077-C-T

16225956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36592807-T-C

16236253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36585089-G-A

16236541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584815-A-T

16236597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584761-A-G

http://identifiers.org/hco/7/GRCh38#16236602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36584756-C-A

16236602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584756-C-G

16236677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584681-C-T

16239689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581594-G-A

16239689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581594-G-C

16239998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581280-A-G

16240060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581218-A-G

16240469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36580830-A-T

16240713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36580621-T-A

16240721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36580614-G-C

http://identifiers.org/hco/7/GRCh38#16240784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36580540-C-A

16240784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36580540-C-T

http://identifiers.org/hco/7/GRCh38#16241345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36579935-C-A

16241345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579935-C-T

16241590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579691-A-G

16241628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579656-T-C

http://identifiers.org/hco/7/GRCh38#16241639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36579642-A-C

16241669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579615-T-C

16241802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579484-T-C

16241831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579453-T-G

16241854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579425-T-A

16241948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579346-T-C

16244007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36576041-C-G

16244168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575890-G-T

16244186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575872-A-T

16244204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575859-C-T

http://identifiers.org/hco/7/GRCh38#16256945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36573693-C-A

16256982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573657-A-G

16257016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573616-T-C

16257016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573616-T-G

16257079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573555-T-C

16257101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573533-C-T

16257306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573358-T-C

http://identifiers.org/hco/7/GRCh38#16257439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36573225-A-C

16257600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573052-T-C

16257653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573001-G-C

16257653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573001-G-T

16257805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572787-T-A

16258009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572416-G-A

16258199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572227-A-G

16258369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572068-A-G

16258440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36571998-T-C

http://identifiers.org/hco/7/GRCh38#16258501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36571938-A-C

16258501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36571938-A-T

16258819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36571627-A-G

16258819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36571627-A-T

http://identifiers.org/hco/7/GRCh38#16258871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36571571-C-A

16258871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36571571-C-T

16258956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36571486-G-C

16258956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36571486-G-T

http://identifiers.org/hco/7/GRCh38#16259108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36571329-A-C

16259108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36571329-A-T

http://identifiers.org/hco/7/GRCh38#16259124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36571313-A-C

16259124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36571313-A-T

http://identifiers.org/hco/7/GRCh38#16259144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36571299-A-C

16259144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36571299-A-G

16259144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36571299-A-T

16259354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36571079-G-A

16259770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36570556-T-C

16260052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36570280-A-G

16260052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36570280-A-T

16263871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36567524-C-T

http://identifiers.org/hco/7/GRCh38#16264082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36567312-C-A

16264181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36567214-A-G

16264183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36567212-C-T

16264431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566982-T-A

16264476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566943-A-G

16264583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566844-A-G

16264682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566745-G-T

http://identifiers.org/hco/7/GRCh38#16264775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36566618-C-A

16264775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566618-C-G

16264775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566618-C-T

16264961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566447-A-T

16265006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566411-G-T

16265007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566410-C-T

16265078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566354-G-C

16265251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566183-G-A

16265255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566179-T-C

16265292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566132-C-T

16265407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566020-A-G

16265867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36565659-A-G

16265870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36565656-A-G

http://identifiers.org/hco/7/GRCh38#16266022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36565530-C-A

16266086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36565486-G-T

16266278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36565303-T-C

16266279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36565302-G-T

http://identifiers.org/hco/7/GRCh38#16266280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36565301-C-A

16266312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 36565256-G-A

16266312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 36565256-G-T

16266341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36565227-A-G

16266341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36565227-A-T

16266345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36565223-T-C

http://identifiers.org/hco/7/GRCh38#16266349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36565219-A-C

16267243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36564965-G-C

16268828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36563421-T-C

16268888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36563374-G-A

16268888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36563374-G-T

16268956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36563301-C-T

http://identifiers.org/hco/7/GRCh38#16268959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36563298-A-C

16268961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36563296-T-G

16268987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36563271-T-C

http://identifiers.org/hco/7/GRCh38#16269301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36562954-A-C

16269301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562954-A-T

16269307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562948-A-G

16269342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36562913-C-T

16269400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562843-A-G

16269445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562817-G-A

16269445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562817-G-C

http://identifiers.org/hco/7/GRCh38#16269492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36562770-A-C

16269617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562678-G-A

16269617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562678-G-C

16269639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562656-G-A

16269639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562656-G-T

16269646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562649-G-C

16269682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562617-G-T

16269683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562616-T-C

http://identifiers.org/hco/7/GRCh38#16269713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36562587-A-C

16269713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562587-A-G

16269757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562544-C-G

16269757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562544-C-T

16269775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562526-G-T

16269796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562505-A-G

16269901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562414-G-T

16269914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562401-T-C

http://identifiers.org/hco/7/GRCh38#16269945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36562368-C-A

16269945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562368-C-T

16270001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562302-A-G

16270002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36562301-T-C

16270090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36561474-G-T

16270154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36561410-T-C

16270197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36561359-A-T

16270223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36561334-T-C

16270238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36561319-G-T

16270335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36561167-T-C

16270356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36561147-G-A

http://identifiers.org/hco/7/GRCh38#16270390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36561118-C-A

16270494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36561025-T-G

16270498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36561021-T-C

http://identifiers.org/hco/7/GRCh38#16270526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36560994-C-A

16270694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36560778-G-T

16270749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36560728-T-C

16271238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36560181-C-T

16271285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36560134-T-C

http://identifiers.org/hco/7/GRCh38#16271644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36559792-A-C

16271718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36559723-T-C

16272133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36557588-T-G

16272729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36556985-A-G

16274462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36556655-G-A

16277620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36553370-C-G

16277870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36553129-G-C

16277887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36553115-G-C

16277995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552192-G-A

16277995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552192-G-T

http://identifiers.org/hco/7/GRCh38#16277996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36552191-A-C

16278020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552168-A-G

16278070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552122-T-C

16278083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552109-G-A

16278083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552109-G-C

16278083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552109-G-T

16278120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36552078-A-G

http://identifiers.org/hco/7/GRCh38#16278257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36551935-C-A

16278257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551935-C-T

16278297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551900-A-T

16278309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551888-T-C

16278323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551874-G-A

16278323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551874-G-T

16278332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551865-T-C

16278332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551865-T-G

16278462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551726-C-G

16278729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551516-G-T

16278786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551469-T-A

16278786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551469-T-C

16278786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551469-T-G

16278817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551438-A-G

16278873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551384-T-C

16278873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551384-T-G

16278877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551380-G-A

16279065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551338-T-G

16279249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551184-T-G

16279308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36551125-A-G

http://identifiers.org/hco/7/GRCh38#16279317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36551116-A-C

16279540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550481-G-T

16279561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550453-A-G

16279647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550367-T-C

16279669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550363-G-A

16279703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550329-G-A

http://identifiers.org/hco/7/GRCh38#16279724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36550308-C-A

16279770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550264-G-A

16279780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36550251-G-A

16282658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36547986-G-A

16282902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36547720-T-C

16282951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36547675-T-C

16282985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36547641-C-T

16283058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36547570-T-C

16293231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36544000-A-G

16293454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36543659-T-C

http://identifiers.org/hco/7/GRCh38#16293481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36543633-C-A

16293646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36543491-A-G

16293660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36543477-T-C

http://identifiers.org/hco/7/GRCh38#16293664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36543473-C-A

16293664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36543473-C-T

http://identifiers.org/hco/7/GRCh38#16293720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36543429-A-C

16293720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36543429-A-G

16293771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36543378-C-G

16293808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36543341-G-T

16294284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36536064-T-C

16294349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535995-G-C

16294349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535995-G-T

16294599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535742-T-C

16294630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535709-A-T

http://identifiers.org/hco/7/GRCh38#16294819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36535523-A-C

16294823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535519-T-C

16294877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535467-T-C

16294988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535365-A-G

16295000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535353-T-C

16295067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535285-T-A

16295121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535227-T-C

16295145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535203-T-G

http://identifiers.org/hco/7/GRCh38#16295175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36535160-C-A

16295175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36535160-C-G

16295457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36533888-C-T

16296095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36533222-G-T

16296178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36533137-T-C

16296268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36533059-T-C

16296268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36533059-T-G

16296378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36532952-A-G

16296378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36532952-A-T

16296644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36532689-C-T

http://identifiers.org/hco/7/GRCh38#16296731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36532614-A-C

16299230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36528804-G-A

16299567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36528476-A-T

16299647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36528398-A-T

16300040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36528064-T-G

16300074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36528029-T-C

16300331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36527802-T-C

16300392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36527744-G-C

16300622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36527514-A-G

16300727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36527427-G-A

16300952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36527211-G-A

16300953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36527210-T-A

16300953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36527210-T-C

16301157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526996-C-G

16301188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526970-A-G

16301263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526898-A-T

16301301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526862-G-C

16301308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526852-G-T

http://identifiers.org/hco/7/GRCh38#16301309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36526851-C-A

16301309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526851-C-T

16301354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526807-A-G

16301358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526803-G-A

16301358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526803-G-T

16301389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526774-A-G

16301389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526774-A-T

16301390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526773-C-T

http://identifiers.org/hco/7/GRCh38#16301416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36526747-C-A

16301416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526747-C-T

http://identifiers.org/hco/7/GRCh38#16301490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36526673-A-C

16301491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526672-G-A

16301491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526672-G-T

16301498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526665-C-T

16301541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526623-G-A

16301541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526623-G-T

16301583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526583-A-G

16301583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526583-A-T

16301744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526424-G-A

16301932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526198-C-T

16301984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526148-A-G

16302025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526107-T-C

16302029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36526103-C-G

http://identifiers.org/hco/7/GRCh38#16302345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36526065-C-A

http://identifiers.org/hco/7/GRCh38#16302513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36525912-A-C

16302523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525902-T-C

16302527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525898-A-G

http://identifiers.org/hco/7/GRCh38#16308389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36523327-C-A

16308389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36523327-C-G

16308391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36523325-A-G

http://identifiers.org/hco/7/GRCh38#16308445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36523280-C-A

16308445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36523280-C-T

16308458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36523267-A-G

16308458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36523267-A-T

16308462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36523263-A-G

16308462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36523263-A-T

http://identifiers.org/hco/7/GRCh38#16308471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36523253-C-A

16308501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36523222-A-G

http://identifiers.org/hco/7/GRCh38#16308621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36523105-C-A

16308621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36523105-C-G

16308621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36523105-C-T

16308676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36523031-A-G

16308724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36522973-G-C

16308724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36522973-G-T

http://identifiers.org/hco/7/GRCh38#16308725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36522972-C-A

16308853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36522872-T-C

16308853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36522872-T-G

16308996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36522756-G-A

16309022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36522727-T-C

16309048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36522705-A-G

16309052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36522701-C-T

http://identifiers.org/hco/7/GRCh38#16309138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36522611-A-C

16309257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36522498-C-G

http://identifiers.org/hco/7/GRCh38#16317901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36519887-A-C

16317946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36519847-A-G

16318205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36519589-T-A

16318205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36519589-T-C

16318514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36519097-G-C

16318514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36519097-G-T

16318603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36519029-T-C

16318610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36519022-C-T

16318677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518947-A-T

16318692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518933-C-G

16318785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518847-C-T

http://identifiers.org/hco/7/GRCh38#16318976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36518575-C-A

http://identifiers.org/hco/7/GRCh38#16319075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36518465-A-C

16319175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518364-A-G

16319323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518231-G-A

16319341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518213-A-G

16319385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518169-G-C

16319411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518146-A-T

16319415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518142-G-A

16319445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518117-T-C

16319481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518081-G-A

16319489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518073-T-C

16319690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517902-G-A

16319693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517899-A-T

http://identifiers.org/hco/7/GRCh38#16319696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36517896-A-C

16319716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517877-T-C

16319736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517857-T-C

16320007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517696-A-G

16320038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517665-C-T

16320165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517530-T-C

16321214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36516475-A-G

http://identifiers.org/hco/7/GRCh38#16321817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36515948-C-A

http://identifiers.org/hco/7/GRCh38#16323774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36509351-A-C

16323791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36509334-G-C

16323799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36509326-A-T

16324029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36509127-A-T

16324600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36508476-C-G

16324601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36508475-T-C

16324622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36508449-A-T

16324637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36508424-T-C

16324663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36508398-G-C

http://identifiers.org/hco/7/GRCh38#16324944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36508136-A-C

http://identifiers.org/hco/7/GRCh38#16324989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36508079-C-A

16325328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507804-G-A

16325430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507721-T-C

http://identifiers.org/hco/7/GRCh38#16325478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36507673-C-A

16325549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507605-C-G

16326473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507502-C-T

16326478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507497-G-A

http://identifiers.org/hco/7/GRCh38#16326549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36507423-C-A

http://identifiers.org/hco/7/GRCh38#16326574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36507397-C-A

16326578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507393-A-T

http://identifiers.org/hco/7/GRCh38#16326654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36507316-A-C

16326660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507309-T-A

16326660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507309-T-C

16326750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507233-G-C

16326755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507229-C-T

16326797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507188-C-G

16326797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507188-C-T

16326880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507118-G-A

16326880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507118-G-C

16326961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507042-T-C

16326979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507033-G-A

16326979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36507033-G-C

16353843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36493092-C-G

16353936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36493014-T-C

16353957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492995-C-G

16353981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492970-T-C

16354065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492920-A-T

16354556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492366-A-G

16354556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492366-A-T

16354706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492221-G-T

16354770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492154-A-G

16354900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36492028-A-G

http://identifiers.org/hco/7/GRCh38#16355228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36491766-A-C

16355260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36491734-G-A

16355269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36491725-C-G

16355269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36491725-C-T

16355549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36491540-G-C

16355612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36491472-G-C

16355835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36491283-G-A

16355844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36491268-G-C

16356112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36490775-G-A

16356472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36490409-C-T

16356534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36490351-G-C

16356972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36489982-G-A

16356998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36489956-A-G

16359328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36487323-G-T

http://identifiers.org/hco/7/GRCh38#16359481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36487156-C-A

16359492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36487146-G-A

http://identifiers.org/hco/7/GRCh38#16359587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36487057-C-A

16359591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36487053-T-C

16359620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36487007-T-C

16359665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36486971-C-T

16359800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36486832-C-T

16359825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36486807-G-A

16359825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36486807-G-C

16359909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36486599-T-C

16364943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36485803-A-G

16367686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36484389-G-A

16367686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36484389-G-C

16367752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36484324-G-A

16367752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36484324-G-T

16367778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36484303-C-T

16367854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36484245-A-G

http://identifiers.org/hco/7/GRCh38#16368036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36484057-C-A

16368041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36484052-T-C

16368433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36483659-T-C

16368480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36483598-T-C

16368513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36483563-T-C

16368651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36483425-C-T

16368659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36483418-T-C

http://identifiers.org/hco/7/GRCh38#16368726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36483356-A-C

16368811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36483268-A-G

16375251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36477264-C-T

16375304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36477221-G-A

16375500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36477024-A-G

16375603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36476923-C-T

16375773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36476752-C-T

16375984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36476550-A-G

16376011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36476524-G-A

16376011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36476524-G-T

16376076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36476451-A-G

16376171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36476356-G-A

16376213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36476314-G-C

16376257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36476266-G-A

http://identifiers.org/hco/7/GRCh38#16376261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36476262-A-C

16376261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36476262-A-G

16376299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36476223-T-A

http://identifiers.org/hco/7/GRCh38#16376307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36476215-C-A

16376389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36476134-A-T

16376442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36476056-C-T

16376506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36475816-A-T

http://identifiers.org/hco/7/GRCh38#16376508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36475815-C-A

16376623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36475692-A-T

16376624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36475691-G-A

16376879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36475434-A-G

16376979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36475335-T-C

http://identifiers.org/hco/7/GRCh38#16376998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36475316-C-A

16377025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36475286-C-G

16377357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36475008-G-A

16377519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36474841-G-A

16377722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36474636-G-C

http://identifiers.org/hco/7/GRCh38#16377753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36474603-A-C

16377924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36474464-A-T

16377979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36474414-G-C

16400839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446935-A-G

16400864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446902-C-T

16400911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446843-G-T

16400939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446822-C-T

16400940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446821-A-G

16401004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446757-G-T

16401022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446737-G-A

16401034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446721-T-C

16401035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446720-A-G

16401061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446694-C-T

http://identifiers.org/hco/7/GRCh38#16401099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36446660-C-A

16401326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446429-C-G

16401326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446429-C-T

16401350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446405-G-C

16401377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446380-C-T

16401591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446114-A-G

16401746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445928-C-G

16401821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445861-G-A

16401837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445847-G-A

16401840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445844-T-G

16401852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445826-C-T

16401995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445688-G-A

16401995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445688-G-C

16402107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445581-G-A

16402266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445449-T-A

16402584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445134-T-C

16402732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36444995-T-A

16402819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36444915-A-T

16402905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36444832-G-C

16402971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36444642-G-C

http://identifiers.org/hco/7/GRCh38#16403099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36444417-A-C

16403308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36444236-G-T

16403325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36444219-T-C

http://identifiers.org/hco/7/GRCh38#16403975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36443713-C-A

16403975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36443713-C-G

16404199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36443487-G-C

16404450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36442690-A-G

16404491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36442655-A-G

http://identifiers.org/hco/7/GRCh38#16405931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36440735-C-A

http://identifiers.org/hco/7/GRCh38#16406002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36440675-C-A

16406002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36440675-C-T

16406125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36440555-G-A

16406469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36440215-T-C

16406692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36439830-T-C

16409870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36439062-T-A

16409870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36439062-T-C

16409906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36439023-T-G

16410292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36438722-T-G

http://identifiers.org/hco/7/GRCh38#16410587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36438425-C-A

16410725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36438284-C-T

16410965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36437772-A-G

16410993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36437745-T-G

16411063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36437683-T-C

16411064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36437682-A-G

16411091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36437651-T-C

16411160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36437588-T-C

16411248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36437503-C-T

16411379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36437440-T-C

16411401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36437422-C-T

16411534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36437287-A-G

16411573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36437188-T-G

16412009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36436555-A-G

http://identifiers.org/hco/7/GRCh38#16412333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36436087-A-C

16412421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36435951-C-T

16412667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36435695-G-A

http://identifiers.org/hco/7/GRCh38#16412755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36435607-C-A

16413093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36435276-G-T

16413181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36435190-C-T

16413206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36435167-G-A

16413289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36435103-A-G

16413297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36435095-T-C

16413596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36434834-A-G

16413633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36434798-G-C

16413745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36434727-A-T

16413753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36434719-A-G

16413802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36434668-T-C

16413821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36434631-A-T

16413873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36434581-A-G

16414073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36434462-G-C

16414336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36434229-C-T

16414457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36434161-T-A

16414589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36433508-C-G

16418893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36433142-T-C

16418997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36433039-G-C

16420248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36432566-G-A

16420444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36432423-T-C

16420564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36432316-C-T

16420665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36432244-A-G

16420667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36432243-T-C

16420667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36432243-T-G

16420675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36432235-T-C

16420843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36432066-G-C

http://identifiers.org/hco/7/GRCh38#16421184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#36431903-C-A

16421184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36431903-C-T

16421197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 36431890-G-A

16421197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 36431890-G-C

16421197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 36431890-G-T

16421199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36431888-G-A

16421199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36431888-G-T

16421203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 36431884-G-A

16421203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 36431884-G-C

16421203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 36431884-G-T

16421211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36431876-T-C

http://identifiers.org/hco/7/GRCh38#16421213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36431874-C-A

16421213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36431874-C-T

16421249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36431838-T-C

16421285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36431802-T-C

16421285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36431802-T-G

16421341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36431755-G-A

16421341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36431755-G-C

16421341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36431755-G-T

http://identifiers.org/hco/7/GRCh38#16421344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36431752-C-A

16421344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36431752-C-G

16421344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36431752-C-T

16421363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36431739-A-G

http://identifiers.org/hco/7/GRCh38#16421371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36431721-C-A

16421371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36431721-C-T

http://identifiers.org/hco/7/GRCh38#16421392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36431701-C-A

16421392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36431701-C-T

16421407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36431686-G-A

16421453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36431645-G-A

16421453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 36431645-G-T

16421617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36431542-C-T

16421632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36431527-C-T

16421673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431496-A-G

16421720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431461-C-T

16421788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431403-T-C

16421832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431362-G-A

16421858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431336-A-G

16422065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431141-C-G

16422081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36431122-T-A

16422103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431100-A-T

16422254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36430937-T-A

16422254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36430937-T-C

16422498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36430697-A-T

16422620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36430573-C-G

16422620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36430573-C-T

16422798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36430369-T-C

16433875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414370-A-G

16434093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414145-C-G

16434150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414109-T-C

16434402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36413845-T-C

16434510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413697-C-G

16435190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36409265-T-A

16435327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36409072-G-A

16435518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36408883-A-T

16435587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36408807-C-T

16435808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36408586-C-T

http://identifiers.org/hco/7/GRCh38#16435917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36408271-C-A

16435917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36408271-C-G

16436290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36407094-C-T

16436335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36407039-A-G

16436402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36406968-A-G

16436462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36406912-A-T

16436617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36406747-G-A

16436617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36406747-G-C

16436639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36406728-A-G

16436715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36406648-A-G

16436716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36406647-T-C

16436716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36406647-T-G

16436828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36406298-G-C

16436899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36406238-T-A

16437578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36405443-T-A

16437605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36405418-T-C

16437702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36405330-C-G

16437729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36405303-A-G

16437987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36403907-G-A

16438019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36403871-G-A

16438056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36403838-G-A

16438059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36403835-T-G

16438071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36403821-C-G

16438096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36403714-A-G

16438387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36403415-C-T

16438688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36403107-A-T

16438847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36403034-T-A

16439113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36402761-C-T

16439163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36402711-G-A

16439281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36402579-T-C

16439919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36401713-C-T

16439920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36401712-A-G

16439956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36401669-A-G

16440057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36401566-T-A

16440156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36401476-T-C

16440156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36401476-T-G

16440367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36400907-A-G

16446192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36394839-G-T

16446205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36394821-G-A

16446354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36394683-T-C

16446355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36394682-T-C

16446362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36394675-C-T

16446471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36394578-G-A

16446597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36394459-A-G

16446774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36394291-G-A

16446977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36394086-A-G

16447003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36394054-G-A

16447438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36393844-C-T

16447627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36393672-A-G

16447913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36386083-G-A

16448165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36385885-A-G

16448191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36385870-T-C

16448206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36385857-G-A

16448342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36385722-A-T

http://identifiers.org/hco/7/GRCh38#16448751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36385368-C-A

16448751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36385368-C-T

16448938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36385236-T-C

16449117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36385064-A-G

16449286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36384929-G-C

16449352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36384887-A-G

16449353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36384886-T-A

16449353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36384886-T-C

16449569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36384740-T-C

16449814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36384516-G-T

16449866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36384464-A-G

16449886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36384446-G-T

16450313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36384330-T-C

16450570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36384068-C-T

16451016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36383628-T-C

16451100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36383542-G-T

16451408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36383369-C-T

16451468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36383309-T-G

http://identifiers.org/hco/7/GRCh38#16451637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36383184-A-C

16452178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36382624-C-T

16452254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36382553-C-T

16452393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36382445-G-A

16452393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36382445-G-T

16452593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36382317-G-A

16452867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36382087-T-C

16452880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36382074-G-A

16452958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36382008-T-A

16453241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36381723-T-C

16453276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36381692-T-C

16453293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36381675-C-T

16453550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36381440-A-T

16454078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36378889-G-A

16454257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36378704-C-T

16454505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36378451-T-C

16454593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36378374-C-T

16454830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36378143-A-T

16455483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36377475-G-A

http://identifiers.org/hco/7/GRCh38#16455543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36377419-C-A

16455568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36377399-T-C

16455645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36377322-T-G

16455718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36377031-T-C

16455781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36376974-T-A

16455781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36376974-T-C

16455939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36376815-T-G

16456014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36376735-A-T

http://identifiers.org/hco/7/GRCh38#16457616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36375182-A-C

http://identifiers.org/hco/7/GRCh38#16457624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36375174-C-A

16457631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36375167-G-T

16458008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36374914-C-T

16458104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36374826-A-G

16458265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36374683-A-G

16458341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36374627-T-A

16458367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36374599-T-C

16458395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36374570-G-A

16458464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36374443-A-T

16458571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36371652-G-C

http://identifiers.org/hco/7/GRCh38#16458613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36371610-A-C

16458639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36371584-A-G

16459643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36369934-T-C

16459908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36369724-T-C

16460046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36369586-A-T

16460335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36369377-C-T

16460337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36369375-C-G

16460337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36369375-C-T

16460386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36369354-T-C

16460552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36369270-T-C

http://identifiers.org/hco/7/GRCh38#16460806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36369085-C-A

16461012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36368934-T-G

16461204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36368775-T-G

http://identifiers.org/hco/7/GRCh38#16461374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36368654-C-A

16461374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36368654-C-T

16461486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36368439-C-T

16461966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367976-T-A

16461966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367976-T-G

16461967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367975-G-A

16461991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367952-G-A

16461991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367952-G-T

http://identifiers.org/hco/7/GRCh38#16462011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36367931-C-A

16462056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367888-A-G

16462056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367888-A-T

16462192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367759-G-C

16462192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367759-G-T

16462213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367743-T-C

16462213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367743-T-G

16462236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367723-T-C

16462236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367723-T-G

16462481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367496-G-A

16462481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367496-G-C

16462515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36367462-T-G

16462657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36367335-T-A

16462657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36367335-T-C

16462717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36367275-C-T

16462753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36367239-C-G

16462753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36367239-C-T

http://identifiers.org/hco/7/GRCh38#16462771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36367221-C-A

16462771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36367221-C-T

16462813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36367179-C-G

16463084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36366897-G-C

16463084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36366897-G-T

16463178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36366804-G-T

16463204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36366751-T-G

16463254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36366701-T-C

16463588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36366390-A-G

16463631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36366348-T-C

16463873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36366106-C-G

16464124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365847-T-A

16464142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365829-T-C

16464142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365829-T-G

16464176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365796-G-T

http://identifiers.org/hco/7/GRCh38#16464181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36365791-A-C

16464181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365791-A-T

http://identifiers.org/hco/7/GRCh38#16464216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36365768-A-C

16464351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36365635-A-G

16464355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36365631-A-T

http://identifiers.org/hco/7/GRCh38#16464402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36365586-A-C

16464422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365566-C-T

16464424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365564-G-A

16464424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365564-G-T

16464462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365522-T-A

http://identifiers.org/hco/7/GRCh38#16464501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36365484-A-C

16464501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365484-A-G

16464527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365459-C-T

http://identifiers.org/hco/7/GRCh38#16464611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36365370-A-C

16464668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36365314-C-G

16464992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36364954-T-G

16465623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36364336-T-C

http://identifiers.org/hco/7/GRCh38#16465721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36364239-C-A

16465721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36364239-C-T

16465746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36364213-C-G

16465746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36364213-C-T

http://identifiers.org/hco/7/GRCh38#16465924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36364036-C-A

16465924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36364036-C-T

16465925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36364035-T-C

16465953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36364010-T-C

16465957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36364006-T-C

16465958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36364005-G-T

http://identifiers.org/hco/7/GRCh38#16465999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36363960-C-A

16466107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36363838-T-A

16466855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362863-A-G

16466855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362863-A-T

16467054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362669-A-G

16467359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362392-G-C

16467369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362382-G-A

16467491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362285-A-T

16467638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362143-T-G

16467653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362128-C-T

16467689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36362104-C-G

http://identifiers.org/hco/7/GRCh38#16467725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36362070-A-C

16467802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361996-G-A

16467826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361974-C-T

16467913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361903-G-A

16468400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361761-C-G

16468502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361706-T-G

16468676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361548-A-G

16468750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361479-A-G

16468751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361478-T-C

16468827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361411-G-A

16469007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361237-C-T

16469145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36361136-G-A

16469313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36360973-T-C

16469316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36360970-T-C

16469331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36360958-T-G

16469580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36360789-T-C

16470303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36360455-C-T

16470444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36360303-C-T

16471864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36359377-T-A

16471864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36359377-T-C

16472092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, undefined
orthologous variants: 36359122-T-C

16472147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36359089-G-A

16472323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36358852-T-G

16472324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36358851-G-A

16472324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36358851-G-C

16472825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36358600-T-A

16472825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36358600-T-C

16473143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36358310-T-C

http://identifiers.org/hco/7/GRCh38#16474508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36357487-A-C

16474565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36357430-G-A

16474565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36357430-G-C

16474667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36357329-C-T

16475469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36357054-A-G

16475530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36356996-A-G

16475585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36356937-G-A

16475585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36356937-G-T

16475593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36356928-A-G

16475625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36356901-T-G

16475813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36356717-C-T

16475928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36356620-G-A

16476155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36356296-T-C

http://identifiers.org/hco/7/GRCh38#16476498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36355970-C-A

16476498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36355970-C-G

16476516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36355955-A-G

16476531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36355940-G-A

16476685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36355552-C-T

16476687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36355550-G-A

16476933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36355398-T-C

http://identifiers.org/hco/7/GRCh38#16476947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36355387-C-A

16477414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36354828-G-T

16477415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36354827-C-G

16477415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36354827-C-T

16477419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36354823-C-T

16477698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36354360-A-G

16477791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36354099-T-C

16479083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36353734-C-T

16479170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36353649-A-G

16479251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36353572-T-A

16479272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36353552-A-T

16479373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36353451-G-A

16479611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36353217-T-C

16479856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36352964-G-A

http://identifiers.org/hco/7/GRCh38#16479878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36352942-C-A

16479990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36352811-T-A

16480098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36352698-G-A

16480324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36352465-G-T

16480594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36352211-T-A

16480838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36352034-G-A

16480965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36351925-A-G

16480973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36351917-G-C

16484155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36346967-T-A

16484171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36346946-A-G

16484264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36346853-G-A

16484547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, undefined
orthologous variants: 36346604-C-T

16484872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36346326-G-A

16484900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36346298-G-A

16484918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, undefined
orthologous variants: 36346279-T-C

16484969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36346238-T-C

16484985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36346222-C-G

16485008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, undefined
orthologous variants: 36346199-C-T

http://identifiers.org/hco/7/GRCh38#16485284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36345626-A-C

16485464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36345471-A-G

16485516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36345421-T-A

16485607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36345344-T-G

16485631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36345319-T-C

16485692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36344932-A-G

16485747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36344877-G-T

16485832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36344792-C-T

16485865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36344760-C-T

16485938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36344687-C-T

http://identifiers.org/hco/7/GRCh38#16487103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36344651-C-A

16487191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36344576-A-T

16487204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36344563-C-T

http://identifiers.org/hco/7/GRCh38#16489162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36344442-A-C

16489188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36344415-T-C

16489242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36344366-T-C

http://identifiers.org/hco/7/GRCh38#16489257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36344351-C-A

16491041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36344107-T-C

16491227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36343969-A-G

16491280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36343949-T-A

16491280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36343949-T-C

16491316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36343918-C-T

16491564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36343672-G-C

16491580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36343651-T-C

16491599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36343622-T-C

16491608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36343613-T-G

http://identifiers.org/hco/7/GRCh38#16491653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36343573-C-A

16491783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36343471-A-G

16491995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36343272-G-A

16492121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36343146-G-T

16492253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36343019-T-C

16492310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36342972-G-A

16492384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36342898-T-C

16492490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36342796-G-C

16492692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron_variant, undefined
orthologous variants: 36342613-G-A

16492908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36342383-G-A

16493273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36342123-G-A

16493273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36342123-G-C

16493322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36342078-A-G

16493322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36342078-A-T

16493402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36341986-C-T

16493460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36341933-A-G

16493557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36341851-A-T

16493566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36341842-T-C

16493684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36341715-G-A

http://identifiers.org/hco/7/GRCh38#16494155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36341287-C-A

16494195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36341247-C-G

16494215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36341231-C-G

16494215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36341231-C-T

16494501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36340922-T-C

16494534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36340889-G-A

http://identifiers.org/hco/7/GRCh38#16494663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36340768-A-C

16494663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36340768-A-G

16494934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36340509-T-A

16494934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36340509-T-C

http://identifiers.org/hco/7/GRCh38#16495512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36339852-C-A

16495653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36339684-G-A

16498039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36325140-C-T

16498078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36325118-G-A

16498078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36325118-G-T

16498179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36325024-C-T

16498746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36324631-G-C

16498762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36324615-G-T

16498837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36324539-T-C

16499063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36324329-T-C

16499063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36324329-T-G

16499761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36323960-C-T

16500171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36323545-G-C

16500250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36323464-T-C

16500254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36323460-C-T

16500709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36323056-T-C

16500785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36322984-T-G

16500827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36322942-C-T

16500946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37276
most severe consequence: intron variant
orthologous variants: 36322827-A-G