109912896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 5 prime UTR variant
orthologous variants: 129548941-T-C

109912984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 5 prime UTR variant
orthologous variants: 129548846-T-C

109913045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 5 prime UTR variant
orthologous variants: 129548769-T-C

http://identifiers.org/hco/4/GRCh38#109913134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129548674-C-A

109913134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 5 prime UTR variant
orthologous variants: 129548674-C-T

http://identifiers.org/hco/4/GRCh38#109913159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129548654-C-A

109913342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense variant
orthologous variants: 129548578-C-G

109913342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense variant
orthologous variants: 129548578-C-T

http://identifiers.org/hco/4/GRCh38#109913527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129548400-C-A

109913566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129548359-G-T

109913571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129548354-T-G

109913719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129548237-G-A

109913807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129548143-T-C

109914072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129547925-A-G

109914090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129547906-C-T

109914354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129547608-T-C

http://identifiers.org/hco/4/GRCh38#109914368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129547556-A-C

109914395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129547490-A-G

http://identifiers.org/hco/4/GRCh38#109914532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129547286-C-A

109914553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129547268-A-G

109914567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129547254-C-T

109914969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129546930-A-G

http://identifiers.org/hco/4/GRCh38#109914975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129546924-C-A

109914975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129546924-C-T

http://identifiers.org/hco/4/GRCh38#109915138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129546772-A-C

109915400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129546557-G-C

109915444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129546527-A-G

109915458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129546512-C-T

109915459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129546511-A-G

109915460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129546510-G-A

109915598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129546402-G-A

109916014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129545997-C-G

109916046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129545972-G-A

109916075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129545943-T-C

109916212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129545811-G-A

109916212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129545811-G-T

109916288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129545736-A-G

109916310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129545716-C-T

109916441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129545607-T-C

109916455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129545593-C-T

109916492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129545556-G-A

109921065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129545120-T-C

109921076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129545109-A-G

109921118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129545069-A-G

http://identifiers.org/hco/4/GRCh38#109921208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129544981-C-A

109921635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129544609-T-C

http://identifiers.org/hco/4/GRCh38#109921656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#129544588-A-C

109921676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, undefined
orthologous variants: 129544571-G-A

109923814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129543751-T-A

109923937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129543727-T-G

109924012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129543651-T-C

109924084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129543579-T-A

109924084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129543579-T-C

109927900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129542756-A-G

109928213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129542446-G-T

109930252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129538811-G-A

109930372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129538686-G-T

109930561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129538535-A-G

109930561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129538535-A-T

109930582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129538522-A-G

109930633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129538480-A-G

109930718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129538415-G-A

109930720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129538413-C-T

109930724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129538409-C-T

http://identifiers.org/hco/4/GRCh38#109931008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129538187-C-A

109931008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129538187-C-T

109932101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129537666-G-A

109932153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129537614-T-A

http://identifiers.org/hco/4/GRCh38#109932360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129536950-C-A

109932360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129536950-C-T

109932760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129536883-G-A

109932946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129536751-G-A

109932946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129536751-G-C

109932946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129536751-G-T

http://identifiers.org/hco/4/GRCh38#109932989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129536709-C-A

http://identifiers.org/hco/4/GRCh38#109933096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129536601-C-A

109933096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129536601-C-T

109933154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129536547-G-T

109939717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129535847-G-T

109939730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129535834-T-C

109939981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129535597-C-T

109940159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129535434-C-T

109940661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129533956-T-C

109940701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129533926-A-G

109940748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129533881-T-G

109940756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129533876-A-G

109940756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129533876-A-T

109940776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129533865-G-A

109940776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129533865-G-C

109940776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129533865-G-T

109941023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129533611-T-C

http://identifiers.org/hco/4/GRCh38#109941186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129533443-C-A

109941186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129533443-C-T

109941221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129533408-T-A

109941221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129533408-T-C

109941225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129533404-G-C

109941240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129533312-T-C

http://identifiers.org/hco/4/GRCh38#109941290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129533266-C-A

109941290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129533266-C-T

http://identifiers.org/hco/4/GRCh38#109941360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129533195-A-C

109941480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129533115-T-G

109941591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129533016-A-G

109941636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129532948-C-T

109941844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129532734-G-A

109941952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129532636-T-G

109941988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129532591-T-A

109942160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129532427-C-T

109942263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129532314-T-C

109942300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129532279-A-G

109942540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129532080-T-G

109942559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129532061-A-G

109942586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129532034-C-T

http://identifiers.org/hco/4/GRCh38#109942604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129532017-A-C

109942712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129531917-G-T

109942775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129531865-G-T

109942786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129531853-G-A

109943003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129531454-G-A

109943016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129531441-T-C

109943179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129531292-T-C

http://identifiers.org/hco/4/GRCh38#109943187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129531284-A-C

109943222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129531252-A-G

109943347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129531130-A-G

109943374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129531103-T-A

109943374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129531103-T-C

109943392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129531085-G-A

109943431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129531046-G-A

http://identifiers.org/hco/4/GRCh38#109943485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129530957-A-C

109943661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129530805-T-C

109943694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129530774-A-G

109943694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129530774-A-T

http://identifiers.org/hco/4/GRCh38#109943746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129530724-C-A

http://identifiers.org/hco/4/GRCh38#109943808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129530662-C-A

109943808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129530662-C-G

109943900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129530570-G-T

109944032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense variant
orthologous variants: 129530441-G-C

109944038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense variant
orthologous variants: 129530435-G-A

109944038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense variant
orthologous variants: 129530435-G-C

109944083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129530390-T-C

109944528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129530250-T-G

109944564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129530214-T-A

109944696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129530056-T-C

109944796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129529970-T-C

http://identifiers.org/hco/4/GRCh38#109944816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129529950-C-A

109945020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129529723-A-G

http://identifiers.org/hco/4/GRCh38#109945030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129529713-C-A

109945030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129529713-C-G

109945030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129529713-C-T

109945033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129529710-A-G

109945106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: synonymous_variant, undefined
orthologous variants: 129529618-C-T

109945176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense variant
orthologous variants: 129529548-G-A

109945281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, undefined
orthologous variants: 129529443-T-C

http://identifiers.org/hco/4/GRCh38#109945339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#129529398-C-A

109945339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, undefined
orthologous variants: 129529398-C-T

109947753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129528469-T-C

109947934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129528291-A-T

109948043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129528147-C-T

109948210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129528003-G-A

109948878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129527635-A-G

109948905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129527608-A-G

109949002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129527517-G-A

109949502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129527319-T-C

109949590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129527245-T-C

109949638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129527206-C-T

109949646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129527197-A-G

109949646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129527197-A-T

109950441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129526553-C-T

http://identifiers.org/hco/4/GRCh38#109950655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129526330-C-A

109950705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129526282-A-T

109950920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129526015-C-G

109952221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129524965-G-C

109952228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129524958-T-C

109952274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129524902-A-G

109952686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129524725-T-G

109952765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129524663-T-C

109953150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129524279-G-A

http://identifiers.org/hco/4/GRCh38#109953507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129523931-A-C

109953551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129523895-A-G

109953685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129523784-C-G

http://identifiers.org/hco/4/GRCh38#109953798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129523676-A-C

http://identifiers.org/hco/4/GRCh38#109954196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129523531-C-A

109954196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129523531-C-T

http://identifiers.org/hco/4/GRCh38#109954199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129523528-A-C

109954199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129523528-A-G

http://identifiers.org/hco/4/GRCh38#109954274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129523511-A-C

109955196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129522597-A-G

109955209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129522584-A-G

http://identifiers.org/hco/4/GRCh38#109955318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129522479-C-A

109955321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129522476-C-T

109955359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129522441-T-A

109955498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129522308-G-C

http://identifiers.org/hco/4/GRCh38#109955878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129521973-A-C

109956442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129521203-G-T

109957606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129519956-G-A

109959354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129518845-C-G

109959354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129518845-C-T

109959376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129518823-G-A

109959842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129517991-A-G

109959966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129517868-G-A

109960725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129517169-G-A

109960725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129517169-G-C

109960725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129517169-G-T

109960765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129517129-T-C

109960770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129517124-G-T

109960801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129517097-T-A

109960801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129517097-T-C

http://identifiers.org/hco/4/GRCh38#109961103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129516810-C-A

109961103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129516810-C-T

http://identifiers.org/hco/4/GRCh38#109961321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129516693-C-A

109961388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129516634-A-G

http://identifiers.org/hco/4/GRCh38#109961407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129516604-A-C

109961449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129516563-T-C

109961981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129513882-T-C

109962108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129513763-A-G

109962217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129513688-C-T

109963261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: synonymous variant
orthologous variants: 129512741-T-C

109963366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129512632-G-A

109963408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129512569-A-G

109963428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129512550-T-C

109963433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129512545-A-G

109963450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129512528-T-A

http://identifiers.org/hco/4/GRCh38#109963648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129512350-A-C

109963654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129512341-T-C

109963911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129512104-G-A

http://identifiers.org/hco/4/GRCh38#109964285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129511820-A-C

109964327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129511778-G-A

109964327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129511778-G-T

109964373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129511736-T-G

http://identifiers.org/hco/4/GRCh38#109964490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129511618-C-A

109964490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: stop gained
orthologous variants: 129511618-C-T

http://identifiers.org/hco/4/GRCh38#109964632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129511485-C-A

109964632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129511485-C-G

109964651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129511467-T-C

109964651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129511467-T-G

http://identifiers.org/hco/4/GRCh38#109968804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129510590-A-C

http://identifiers.org/hco/4/GRCh38#109969029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129510367-A-C

109969156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129510240-G-A

109969156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129510240-G-C

http://identifiers.org/hco/4/GRCh38#109969264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129510137-C-A

109969264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129510137-C-T

http://identifiers.org/hco/4/GRCh38#109969269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129510132-C-A

109969269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129510132-C-G

109969269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129510132-C-T

109970439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129509200-A-G

109971119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129508828-T-C

109971687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129508207-A-T

109972203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129507674-C-G

109972203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129507674-C-T

109974257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129507367-A-G

109974369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129507243-T-C

109974474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506968-A-T

109974570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506843-T-C

109974570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506843-T-G

109974572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506841-G-A

109974572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506841-G-T

109974574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506839-G-C

109974576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506837-G-A

109974578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506835-G-A

109974578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506835-G-T

109974645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506758-T-C

http://identifiers.org/hco/4/GRCh38#109974832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129506576-C-A

109974832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506576-C-G

109974845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506563-G-A

109974848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506560-A-G

http://identifiers.org/hco/4/GRCh38#109974890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129506487-A-C

109974890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506487-A-G

109974915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506462-T-A

109974936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506419-C-T

109975083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129506114-T-C

109975965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129505166-A-G

109976270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129504628-A-G

109976281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129504617-A-G

109976285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129504613-G-T

http://identifiers.org/hco/4/GRCh38#109976316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129504582-C-A

109976316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129504582-C-T

109976391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129504519-A-G

109976422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129504488-G-A

109976469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129504443-A-G

http://identifiers.org/hco/4/GRCh38#109976533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129504372-A-C

109976535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129504351-G-A

109976989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129503759-A-G

109977104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129503649-T-C

109977218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129503530-T-A

109977438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129503300-A-G

109978496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129502448-C-T

109978497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129502447-G-A

109978613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129502355-C-T

109978677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129502290-G-A

109979044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129501927-C-T

109979057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129501914-C-T

109979316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129501608-G-A

http://identifiers.org/hco/4/GRCh38#109979396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129501537-A-C

109979450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129501462-G-A

109979498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129501400-C-G

109979498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129501400-C-T

109979824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129501119-G-A

109979824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129501119-G-C

109979824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129501119-G-T

http://identifiers.org/hco/4/GRCh38#109979830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129501113-C-A

109979830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129501113-C-T

109979938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129501062-G-A

http://identifiers.org/hco/4/GRCh38#109979990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129501005-C-A

109979990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense variant
orthologous variants: 129501005-C-T

109980191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129500806-T-G

109980263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129500728-T-C

http://identifiers.org/hco/4/GRCh38#109980492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129500199-C-A

109980499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129500192-T-C

109980557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129500138-A-G

http://identifiers.org/hco/4/GRCh38#109980567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129500128-C-A

109980567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129500128-C-G

109980567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129500128-C-T

109980618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron variant
orthologous variants: 129500073-T-A

109980698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129500003-T-G

109980811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129499912-T-C

109980888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129499835-A-G

109981125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129499607-T-G

http://identifiers.org/hco/4/GRCh38#109983301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129496340-C-A

109983301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129496340-C-T

109983353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129496297-T-C

109983535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129496118-G-A

109983541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 129496112-G-A

109983541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 129496112-G-C

109983541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 129496112-G-T

http://identifiers.org/hco/4/GRCh38#109983668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129495994-C-A

109983902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129495793-A-G

109985995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129493672-G-A

109986003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129493664-T-C

109986038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129493628-A-G

109986051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129493615-G-T

109986189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129493527-A-G

109986206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129493510-A-G

109986341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129493387-G-A

109986382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129493374-T-C

109986439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129493329-G-C

109986621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129492846-A-G

109986651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129492830-G-A

http://identifiers.org/hco/4/GRCh38#109986768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129492699-A-C

109986797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129492670-C-T

109986879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129492590-A-G

109986916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129492553-T-C

109986980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129492484-A-T

109987091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129492385-A-G

109987097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129492379-T-C

109987660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129491559-A-T

http://identifiers.org/hco/4/GRCh38#109987690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129491534-C-A

109987690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129491534-C-T

109987773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129491452-A-T

http://identifiers.org/hco/4/GRCh38#109987785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129491440-C-A

109987785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129491440-C-G

109987785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129491440-C-T

109987788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129491437-T-C

109987792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129491433-T-C

109987896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129491329-T-C

109987915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129491310-T-C

http://identifiers.org/hco/4/GRCh38#109987942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129491283-C-A

http://identifiers.org/hco/4/GRCh38#109987991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129491238-C-A

109987991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129491238-C-T

109987997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129491232-A-G

http://identifiers.org/hco/4/GRCh38#109988054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129491176-C-A

109988179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129491078-A-G

109988475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129490790-T-A

109988475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129490790-T-C

109988476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129490789-A-G

109988559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129490588-C-G

109988559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129490588-C-T

109988621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 129490526-C-T

109988691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 129490456-G-A

109988794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129490344-A-G

109988794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129490344-A-T

109988800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129490338-T-C

109988836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129490307-G-T

http://identifiers.org/hco/4/GRCh38#109988845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129490298-C-A

109988845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129490298-C-T

http://identifiers.org/hco/4/GRCh38#109989011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129490160-C-A

109989033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129490146-T-A

109989033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129490146-T-G

109989130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129490053-G-A

109989226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129489962-A-G

109989245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129489943-T-G

109989246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129489942-C-T

109989264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129489924-G-T

109989283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129489907-C-G

109989283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129489907-C-T

109989335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129489855-T-C

109989450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129489744-C-G

109989493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129489694-T-A

109990135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129488525-G-C

109990158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129488502-T-C

109990235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129488437-C-T

109990297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129488375-A-G

http://identifiers.org/hco/4/GRCh38#109990318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129488350-A-C

109990344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129488327-A-G

109990479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129488190-G-A

109990494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129488175-A-G

109990513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129488161-G-A

109990613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129488100-G-A

109990614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129488099-G-A

109990640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129488073-C-T

109990911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129487887-C-T

109990952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129487849-G-T

109991010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129487790-G-T

109991213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129487637-A-G

109991443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129487415-T-C

109991524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129487335-G-T

http://identifiers.org/hco/4/GRCh38#109993182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129486750-C-A

109993182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129486750-C-G

http://identifiers.org/hco/4/GRCh38#109993185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129486747-A-C

109993201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129486727-T-G

http://identifiers.org/hco/4/GRCh38#109993428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129486503-C-A

109993438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129486496-T-G

109993501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129486448-T-C

109993513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129486436-T-C

109993513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129486436-T-G

109993516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129486433-G-A

109993527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129486422-T-G

109993744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129485627-A-G

109994050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129485403-A-T

109994846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129484452-A-G

109994871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129484427-A-G

109995439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129483829-T-A

109995526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129483749-C-T

109995651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129482948-G-A

109995656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129482943-T-A

109996118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129482529-T-C

http://identifiers.org/hco/4/GRCh38#109996200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129482438-A-C

109996242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129482407-C-T

109996287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129482369-T-A

109996445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129482124-T-C

http://identifiers.org/hco/4/GRCh38#109996588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129481994-C-A

http://identifiers.org/hco/4/GRCh38#109998270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129481405-A-C

109998443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129481262-A-G

109998468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129481236-G-T

109998593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129481098-G-A

109998728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129480977-A-G

109998728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129480977-A-T

109998927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129480855-G-T

109999204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129480564-C-T

109999256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129480512-A-G

http://identifiers.org/hco/4/GRCh38#109999312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129480459-C-A

109999612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129480061-G-A

109999677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 129480001-A-G

109999707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129479971-T-C

109999862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129479817-C-T

http://identifiers.org/hco/4/GRCh38#110000407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129479546-A-C

110000407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129479546-A-T

110000425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129479528-A-G

110000441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129479512-A-G

110000743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129479234-A-G

110000747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129479230-A-G

110001059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129478946-C-T

110001107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129478900-T-C

110001204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129478809-T-C

110001292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129478730-C-G

110001292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129478730-C-T

110004440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129477027-A-G

http://identifiers.org/hco/4/GRCh38#110004442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129477025-C-A

110004442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129477025-C-T

110004555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129476908-G-A

110004583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129476877-T-C

110004588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129476872-C-T

110004673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129476791-T-C

110006510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129476623-A-G

110006601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129476544-G-A

http://identifiers.org/hco/4/GRCh38#110006675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129476485-C-A

110006780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129476361-T-C

110006865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129476269-G-T

110006955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129476179-T-C

110006973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129476157-G-T

110007133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129476003-G-C

110007237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129475894-A-G

110007356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129475786-G-T

110007397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129475745-T-C

110007497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129475647-G-A

110007641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129475505-G-C

110007662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129475479-G-A

110007768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129475371-G-T

110007910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129475248-A-G

110008024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474971-G-C

110008024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474971-G-T

110008073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474933-T-A

110008100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474906-T-C

110008141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474862-G-A

110008141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474862-G-T

110008218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 129474785-C-T

110008259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474741-A-G

110008294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474707-A-G

110008295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474706-T-C

110008304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474693-T-A

110008307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474690-T-G

110008340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474666-T-A

110008356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474651-T-C

110008375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474636-T-C

http://identifiers.org/hco/4/GRCh38#110008399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129474617-C-A

http://identifiers.org/hco/4/GRCh38#110008400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129474616-A-C

110008400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474616-A-G

110008412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474593-T-A

110008431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474545-G-A

110008478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474463-G-A

110008547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474382-T-A

110008683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474256-G-A

110008902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129474039-T-C

110008977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129473965-T-C

110009057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129473891-A-G

110009070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129473878-G-A

110009118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129473832-C-G

110009127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129473823-C-T

http://identifiers.org/hco/4/GRCh38#110009159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129473791-A-C

110009244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129473709-C-T

http://identifiers.org/hco/4/GRCh38#110009284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129473680-C-A

110009387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129473584-C-G

110011194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129472223-T-C

110011312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 129472098-A-G

http://identifiers.org/hco/4/GRCh38#110011333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129472077-C-A

110011333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129472077-C-T

110011361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129472056-G-A

110011361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129472056-G-C

110011361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129472056-G-T

110011382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129472040-C-G

110011409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129472013-A-G

110011409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129472013-A-T

110011522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129471912-A-G

http://identifiers.org/hco/4/GRCh38#110011530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129471907-C-A

110011546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129471892-G-A

110011546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129471892-G-C

http://identifiers.org/hco/4/GRCh38#110011597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129471837-C-A

110011597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129471837-C-T

110011601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129471833-G-C

http://identifiers.org/hco/4/GRCh38#110011633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129471776-C-A

http://identifiers.org/hco/4/GRCh38#110011645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129471768-A-C

110011645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129471768-A-T

http://identifiers.org/hco/4/GRCh38#110011721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129471708-A-C

110011740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129471689-T-C

110011786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129471658-G-T

110011827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129471622-G-A

110011827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129471622-G-T

http://identifiers.org/hco/4/GRCh38#110011842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129471607-C-A

110011845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129471604-T-C

110011852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129471597-G-A

110011852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129471597-G-T

110011864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129471585-A-T

http://identifiers.org/hco/4/GRCh38#110011879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129471571-A-C

110011909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129471540-T-A

110011909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129471540-T-C

110011958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129471508-T-G

110011960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129471506-G-T

110012111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129471371-C-T

110012153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 129471316-G-A

110012153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 129471316-G-T

110012275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3 prime UTR variant
orthologous variants: 129471214-T-A

110012275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3 prime UTR variant
orthologous variants: 129471214-T-G

110012290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3 prime UTR variant
orthologous variants: 129471203-G-A

110012852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3 prime UTR variant
orthologous variants: 129471069-G-A

110012906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3 prime UTR variant
orthologous variants: 129471006-T-C

http://identifiers.org/hco/4/GRCh38#110013016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129470915-A-C

110013345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3 prime UTR variant
orthologous variants: 129470636-C-T

110013413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3 prime UTR variant
orthologous variants: 129470562-C-G

110013413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3 prime UTR variant
orthologous variants: 129470562-C-T

110013474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3 prime UTR variant
orthologous variants: 129470517-T-A

110013548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3 prime UTR variant
orthologous variants: 129470440-T-C

110013606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3229
most severe consequence: 3 prime UTR variant
orthologous variants: 129470385-T-C