200260411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136700932-A-G

200260457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136700887-G-A

200260618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136700739-T-G

200260705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136700651-G-A

200261474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136696128-A-G

200261475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136696127-G-T

http://identifiers.org/hco/1/GRCh38#200261625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136695999-A-C

200261923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136695836-G-C

200261942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136695817-G-T

200261953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136695805-C-T

200262192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136695537-C-T

200262207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136695522-G-A

200262241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136695493-G-T

200262548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136694533-A-T

200262642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136694447-T-C

200264582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136693845-T-G

200264777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136693587-T-C

200264996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136693379-G-A

200265054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136693320-G-A

200265159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136693208-G-T

200265270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136693160-T-C

200265540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136693012-G-A

200265564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136692988-C-T

200265719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136692858-A-T

200267422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136690959-T-A

200267483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136690897-C-T

200267485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136690895-T-C

http://identifiers.org/hco/1/GRCh38#200267707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136690043-C-A

200268033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136689716-T-C

200274038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136686095-T-G

200274070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136686063-G-C

http://identifiers.org/hco/1/GRCh38#200274149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136685998-A-C

200274149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136685998-A-G

200274286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136685860-A-G

200274286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136685860-A-T

200274351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136685747-A-G

200274413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136685682-C-G

200274414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136685681-C-T

200274699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136685337-T-C

200274776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136685173-T-C

200275034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136684907-G-A

200275178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136684735-T-G

200275370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136684555-G-A

200275370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136684555-G-T

200275394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136684531-G-A

200275617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136684316-G-C

200275780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136684141-G-A

http://identifiers.org/hco/1/GRCh38#200275986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#136683932-C-A

200276118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136683819-T-A

200276756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136681669-T-C

200276770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136681655-A-T

200277125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680889-T-A

200277125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680889-T-C

200277197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680819-A-G

200277281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680741-T-C

200277340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680688-T-C

200277428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680598-G-A

200277933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679666-G-A

200279807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136677233-C-T

200279820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136677219-T-C

200279827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136677212-C-T

200280103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136676988-T-A

http://identifiers.org/hco/1/GRCh38#200280203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136676893-A-C

http://identifiers.org/hco/1/GRCh38#200292208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136674281-A-C

200292636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136673528-G-A

200292741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136673428-G-A

200292883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136673326-T-C

200292883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136673326-T-G

200293045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136673170-A-T

200293079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136673139-C-T

200293186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136673023-T-C

200293293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672955-C-T

http://identifiers.org/hco/1/GRCh38#200293295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136672953-C-A

200293407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672845-G-A

200293520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672752-T-G

200293522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672750-T-C

200293532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672740-T-C

200293593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672679-C-T

http://identifiers.org/hco/1/GRCh38#200293676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136672610-A-C

200293998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136671860-G-A

200294008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136671858-G-A

200294029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136671837-T-A

200294034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136671832-G-C

200294052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136671814-T-C

200294127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136671723-A-G

200294280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136671577-A-G

200294592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136671343-G-A

200294593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136671342-A-G

200294649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136671285-G-A

http://identifiers.org/hco/1/GRCh38#200294770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136671179-C-A

200296975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

200299736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136661548-C-G

http://identifiers.org/hco/1/GRCh38#200300171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136661161-C-A

http://identifiers.org/hco/1/GRCh38#200302002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136659712-C-A

200303482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136658274-T-C

200305667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136655989-C-G

200305667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136655989-C-T

200305669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136655988-T-C

200305680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136655977-T-C

200306532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136655430-G-A

200306533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136655429-T-G

http://identifiers.org/hco/1/GRCh38#200306602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136655360-C-A

http://identifiers.org/hco/1/GRCh38#200307531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136654226-C-A

200307549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136654208-T-G

200307641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136654108-G-A

http://identifiers.org/hco/1/GRCh38#200307837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136653915-A-C

200308051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136653462-A-T

200308123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136653373-G-A

200308176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136653324-G-T

200309144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136652870-T-C

200309509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136652064-C-G

200309700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136651873-C-T

200309807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136651766-T-C

200309807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136651766-T-G

200312892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136648004-T-C

200313005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136647900-G-A

200313096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136647812-T-C

200313126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136647769-C-T

http://identifiers.org/hco/1/GRCh38#200313157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136647752-C-A

200313174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136647743-T-G

200313258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136647659-G-A

200313518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136647422-A-G

200313811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136647173-G-A

200314073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136646277-T-G

200314185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136646145-G-A

200314185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136646145-G-T

200314209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136646115-G-C

200314342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136646028-A-G

200314370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136646002-G-T

200314466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136645911-C-G

200314522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136645844-T-G

200314703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136645662-T-A

200315395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136644968-C-T

200315521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136644815-C-T

http://identifiers.org/hco/1/GRCh38#200315590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136644742-C-A

200315889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136643681-G-A

200316572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136642959-G-T

200316645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136642887-G-A

200316715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136642817-C-T

200316821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136642711-G-A

200317317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136642413-A-G

200317587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136642160-A-T

200317733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136642000-T-C

200317882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136641800-G-A

http://identifiers.org/hco/1/GRCh38#200320952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136637766-C-A

200332590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136625482-T-C

200332696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136625417-C-T

200336045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136624892-T-C

200336058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136624879-C-T

200336264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136624766-A-G

200336265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136624765-T-C

200336265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136624765-T-G

200336925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136624085-T-C

200336927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136624083-G-A

200337308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136623738-T-C

200338068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136622876-A-G

http://identifiers.org/hco/1/GRCh38#200338254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136622743-A-C

200338310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136622699-G-A

200338383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136622661-G-A

200338930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136621810-G-A

200338950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136621783-C-G

200339583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136621125-G-A

200339673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136621066-C-T

200339676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136621063-C-T

200340601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136619845-G-T

200340672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136619773-C-T

200351839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136614114-T-G

200352605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136612921-G-A

200354145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136611895-C-T

200354169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136611872-C-T

200354567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136611469-A-G

200355945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136610735-C-G

200361379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136606644-T-C

200362586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136604942-C-T

200362717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136604841-G-A

200362934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136604534-T-A

200363166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136604301-T-G

200363263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136604201-T-C

200363505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136603974-G-T

200363727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136603692-A-G

200364262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136602960-C-G

200364326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136602886-T-G

200364452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136602762-G-A

200364648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136602570-T-G

200364927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136602360-G-A

200366073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136600703-T-C

200366073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136600703-T-G

200366649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136600270-T-G

200366650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136600269-G-T

200366698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136600239-G-A

200366708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136600229-G-A

200366708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136600229-G-T

200366734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136600200-G-A

200366734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136600200-G-C

http://identifiers.org/hco/1/GRCh38#200367031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136600021-C-A

200367104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136599977-T-C

200367148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136599962-A-G

200367833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136599691-C-T

200367963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136599574-A-G

200368310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136599268-C-T

200368318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136599260-C-T

http://identifiers.org/hco/1/GRCh38#200368664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136599015-C-A

200368664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 136599015-C-G

200368664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 136599015-C-T

http://identifiers.org/hco/1/GRCh38#200368688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136598993-C-A

200368688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598993-C-G

200368688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598993-C-T

200368689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598992-A-G

200368689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598992-A-T

200368707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598975-A-G

200368717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598965-G-A

200368717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598965-G-T

200368742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598941-T-C

200368742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598941-T-G

200368744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598939-G-A

200368744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598939-G-T

http://identifiers.org/hco/1/GRCh38#200368773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136598910-C-A

200368773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598910-C-T

200368795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598841-G-A

200368795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598841-G-T

200368805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598826-G-A

200368805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598826-G-T

200368826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598753-G-A

200368826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598753-G-C

200368826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136598753-G-T

200368877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136598717-A-G

200368877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136598717-A-T

200369005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136598614-C-T

200369105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136598514-T-C

200369218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136598406-T-C

http://identifiers.org/hco/1/GRCh38#200369423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136598282-A-C

200369423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136598282-A-G

200369462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136598247-C-T

200369555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136598158-G-C

200369754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136597968-C-T

200369815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136597908-C-T

200369905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136597819-G-A

200369947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136597778-G-A

200370039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136597686-C-G

200370048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136597678-T-A

200371530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136596200-T-C

200371816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136593601-G-A

200372146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136593262-C-T

200372836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136592841-T-C

200372892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136592779-A-G

200372988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136592687-G-T

http://identifiers.org/hco/1/GRCh38#200373010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136592666-C-A

200373010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136592666-C-G

200373243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136592427-T-C

200373283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136592390-C-T

200373289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136592384-C-T

200373467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136591689-T-C

200373472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136591684-G-A

200373812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136590202-T-C

200374646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136589396-G-A

200374827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136589231-G-A

200374830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136589228-T-C

200375009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136589041-G-C

200375812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136588015-G-A

200375969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136587897-T-G

200376000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136587869-C-G

200376248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136587636-A-G

200377304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136586515-G-T

200377398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136586458-G-C

200377684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136586197-C-T

200377685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136586196-A-G

200377748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136586142-T-C

200377882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136586020-G-A

200377882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136586020-G-T

200377911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136585971-T-A

200377953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136585926-C-T

http://identifiers.org/hco/1/GRCh38#200377955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136585924-C-A

200378361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136585400-T-C

http://identifiers.org/hco/1/GRCh38#200379357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136584712-C-A

200379486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136584582-T-G

200379631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136584453-G-A

http://identifiers.org/hco/1/GRCh38#200380489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#136583481-C-A

200380672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136583293-T-C

200380702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136583264-G-A

200380920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136582953-G-A

200380920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136582953-G-C

200380994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136582863-T-C

200381159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136582597-C-T

200381327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136582423-C-T

http://identifiers.org/hco/1/GRCh38#200381405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136582345-C-A

200382005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136581844-A-G

200382564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136581620-C-T

200382661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136581533-C-T

200382705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136581495-G-A

200382705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136581495-G-T

http://identifiers.org/hco/1/GRCh38#200383220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136580937-A-C

200383478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136580601-A-G

http://identifiers.org/hco/1/GRCh38#200385461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136579293-A-C

200387521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136574272-T-C

200387812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136573687-C-T

200387943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136573489-C-T

http://identifiers.org/hco/1/GRCh38#200388037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136573417-C-A

200388038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136573416-A-T

200388938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136572428-T-G

http://identifiers.org/hco/1/GRCh38#200389194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136572207-A-C

200389194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136572207-A-G

200389270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136572145-T-G

http://identifiers.org/hco/1/GRCh38#200391678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136567169-C-A

200391678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136567169-C-T

http://identifiers.org/hco/1/GRCh38#200391906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136566810-C-A

200391915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136566801-G-A

http://identifiers.org/hco/1/GRCh38#200392043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136566679-C-A

200392161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136566401-T-A

200392231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136566272-G-T

200392496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136565843-T-G

200392563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136565787-T-C

200398864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136563386-T-C

200398952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136563301-C-T

200399040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136563211-T-C

http://identifiers.org/hco/1/GRCh38#200399106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136563144-A-C

200399695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136562557-T-C

200399921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136562331-T-C

200400193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136562036-A-T

200400225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136562010-A-G

200400225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136562010-A-T

http://identifiers.org/hco/1/GRCh38#200400643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136561728-C-A

200400678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136561689-A-G

http://identifiers.org/hco/1/GRCh38#200400704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21901
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136561665-C-A