http://identifiers.org/hco/6/GRCh38#112236337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38856990-C-A

112236415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38856918-T-A

112236415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38856918-T-C

112236488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38856852-T-C

112236677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38856404-C-T

112236682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38856399-G-A

112236803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38856292-T-C

http://identifiers.org/hco/6/GRCh38#112236829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38856270-C-A

112236829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38856270-C-T

http://identifiers.org/hco/6/GRCh38#112237203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38855896-C-A

112237291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38855827-G-A

http://identifiers.org/hco/6/GRCh38#112237394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38855740-A-C

112237501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38855635-A-T

112237837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38855363-G-T

http://identifiers.org/hco/6/GRCh38#112237898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38855303-A-C

112238053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38855174-T-G

112238131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38855101-G-T

112238199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38855035-T-C

112238287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38854915-G-A

112238292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38854910-C-G

http://identifiers.org/hco/6/GRCh38#112238318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38854868-A-C

http://identifiers.org/hco/6/GRCh38#112238388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38854798-C-A

112238819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38854673-T-C

112238895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38854620-C-T

112239541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38854140-C-T

112241681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38853334-C-G

112242083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38852859-C-G

112242083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38852859-C-T

112242420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38852462-A-G

112242479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38852379-C-T

112242608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38852267-A-G

112242671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38852206-T-C

112242671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38852206-T-G

112242700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38852182-C-T

112242745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38852142-T-A

112242881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38851992-T-C

112243044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38851879-G-A

112243044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38851879-G-T

112243136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38851778-T-C

112243237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38851667-T-A

http://identifiers.org/hco/6/GRCh38#112243242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38851662-C-A

112243285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38851598-C-T

112243378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38851509-T-A

112243378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38851509-T-C

112243601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38851304-C-T

112243682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38851223-G-C

112244748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38850996-T-C

http://identifiers.org/hco/6/GRCh38#112244814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38850933-A-C

http://identifiers.org/hco/6/GRCh38#112244920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38850810-A-C

112245113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38850609-G-C

http://identifiers.org/hco/6/GRCh38#112245176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38850550-A-C

112245663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38849669-A-G

112245849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38849452-T-C

112245859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38849435-T-G

112246183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38849103-C-T

112246884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38848695-C-T

112246885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38848694-C-T

112246924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38848655-A-G

112247126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38848459-G-A

112247135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38848450-G-A

112247406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38848014-T-C

112247467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38847736-G-A

112247470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38847733-A-G

http://identifiers.org/hco/6/GRCh38#112247533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38847509-A-C

http://identifiers.org/hco/6/GRCh38#112247649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38847396-C-A

112249460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38846838-A-G

112249669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38846669-T-C

112249799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38846603-C-G

112250120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38846317-G-C

112250352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38846097-G-A

112250643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38845823-C-T

112250656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38845810-C-T

112250687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38845778-C-G

http://identifiers.org/hco/6/GRCh38#112250733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38845738-C-A

112250866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38845608-A-G

112250934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38845306-T-C

112250938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38845302-T-C

112251083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38845159-G-T

112251149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38845095-G-A

112251310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38844946-G-T

http://identifiers.org/hco/6/GRCh38#112251453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38844824-C-A

112251453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38844824-C-T

http://identifiers.org/hco/6/GRCh38#112251714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38844566-C-A

112251714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844566-C-T

112251715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844565-G-A

112251715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844565-G-T

112251717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844563-T-C

112251750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844532-G-A

112251761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844521-A-G

112251806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844486-A-G

112251810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844482-T-C

112252130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844188-A-G

112252159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844177-A-G

112252455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38843911-T-C

112252722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38843665-G-C

112252842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38843559-A-G

112252874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38843520-T-C

http://identifiers.org/hco/6/GRCh38#112253026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38843312-C-A

112253026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38843312-C-G

112253228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842839-G-T

112253349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842721-A-T

112253409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842649-G-A

112253409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842649-G-C

112253409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842649-G-T

http://identifiers.org/hco/6/GRCh38#112253536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38842528-C-A

112253536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842528-C-G

http://identifiers.org/hco/6/GRCh38#112253590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#38842470-C-A

112253590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38842470-C-T

112253618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842442-T-G

http://identifiers.org/hco/6/GRCh38#112253693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38842371-C-A

112253693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842371-C-G

112253693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842371-C-T

112253782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38842308-T-C

112253973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38842126-G-C

http://identifiers.org/hco/6/GRCh38#112253988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#38842111-C-A

112253988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38842111-C-T

112253989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38842110-G-A

http://identifiers.org/hco/6/GRCh38#112254028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#38842071-C-A

112254028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38842071-C-G

112254028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38842071-C-T

112254091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38842008-G-A

112254091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38842008-G-C

112254151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841948-T-A

112254172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841927-T-G

112254183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841915-G-A

112254183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841915-G-T

112254195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841903-G-A

http://identifiers.org/hco/6/GRCh38#112254217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#38841879-C-A

112254256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841842-G-A

112254256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841842-G-C

112254256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841842-G-T

112254259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841839-T-A

112254260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841838-G-A

112254260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841838-G-C

112254307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841788-G-A

112254307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841788-G-C

112254324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841771-G-T

http://identifiers.org/hco/6/GRCh38#112254389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#38841730-C-A

112254389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841730-C-T

112254433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841677-A-G

112254461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 38841649-T-C

112254476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841631-C-T

http://identifiers.org/hco/6/GRCh38#112254479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#38841624-A-C

112254479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841624-A-G

112254555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841547-T-A

112254555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38841547-T-G

http://identifiers.org/hco/6/GRCh38#112254989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38841130-C-A

112254989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38841130-C-T

http://identifiers.org/hco/6/GRCh38#112255291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38840826-A-C

112255362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38840756-C-G

112255362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38840756-C-T

http://identifiers.org/hco/6/GRCh38#112255710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38840443-A-C

112255749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38840404-A-G

112256560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38839666-T-C

112256674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38839556-T-C

112256739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38839437-C-G

112256813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839364-T-C

http://identifiers.org/hco/6/GRCh38#112256846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38839303-C-A

112256846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839303-C-T

112256872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839279-T-G

112256884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839267-T-A

112256884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839267-T-C

http://identifiers.org/hco/6/GRCh38#112256960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38839207-C-A

112256960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839207-C-T

112257004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38839112-G-A

112258721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38838880-G-A

112258767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38838833-T-G

112258813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38838784-C-T

112262607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38836081-A-T

112262682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38836004-G-T

112263005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38835674-G-A

112266004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38834135-C-T

112266665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38826062-G-T

112266724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38825992-T-C

112267197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38825326-C-G

112267334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38825214-T-C

112267529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38825011-T-C

http://identifiers.org/hco/6/GRCh38#112267921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38824448-A-C

112268063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38824297-G-A

112268260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38824063-T-C

112268373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38823978-A-G

112268377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38823974-T-C

112268384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38823967-A-T

112268941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38823495-A-T

112268957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38823479-C-T

112269440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38823015-T-C

112269606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38822861-G-A

112269758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38822791-G-A

http://identifiers.org/hco/6/GRCh38#112270381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38822289-C-A

112270422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38822247-T-A

112270428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38822241-A-G

112270593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38805640-A-G

112270626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38805608-C-T

112270647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38805587-A-G

112270674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38805561-T-C

112271032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38805382-G-A

112271058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38805359-T-C

112271066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38805351-T-G

112271278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38805160-G-A

112271278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38805160-G-T

112271281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38805157-C-T

112271457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38804990-T-C

112271457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38804990-T-G

112271617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38804813-A-G

112271622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38804808-T-C

112274012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801975-A-G

112274322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801680-T-C

112274424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801578-G-A

112274657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801371-C-G

112274680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801350-G-A

112274681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801349-A-G

http://identifiers.org/hco/6/GRCh38#112274827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38801206-C-A

112274827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801206-C-G

112274827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801206-C-T

112274950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38801097-C-T

112275926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38799830-C-T

112275966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38799796-T-C

112275966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38799796-T-G

112276111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38799670-C-T

112276253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38799541-A-G

112278034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

112278034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

112278061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

http://identifiers.org/hco/6/GRCh38#112278135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

112278223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

112278234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

112279386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38792504-A-T

112279399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38792490-A-G

112279557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38792377-G-T

112279696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38792257-C-T

112279862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38792092-A-T

112280021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38791942-A-G

112280185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38791759-G-A

112280384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38791138-T-C

112280407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38791112-G-A

112280407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38791112-G-T

112280772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38790496-C-T

112280844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38790422-C-T

112281028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38790315-T-G

112281092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38790256-T-C

112281342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38790057-T-C

112281402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38789996-A-G

112282072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38789530-A-G

112282149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38789462-A-T

112282330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38789329-G-A

112282410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38789220-T-A

112282422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38789209-G-A

112283076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38788399-G-A

112283081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38788389-C-T

112283287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38788210-A-G

112283288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38788209-T-A

112283299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38788198-G-A

112283299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38788198-G-T

112283327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38788170-A-G

112283379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38787936-G-A

112283435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38787873-A-G

http://identifiers.org/hco/6/GRCh38#112283472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38787836-C-A

112285711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38787221-G-T

http://identifiers.org/hco/6/GRCh38#112286151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38786940-C-A

112286191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38786897-T-A

112286193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38786895-A-G

112286311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 38786771-G-A

112286313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 38786769-C-T

112286417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 38786671-A-G

112286756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38786336-T-C

112286867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38786247-T-C

112286926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38786188-T-C

112286927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38786187-G-A

112287128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38786070-C-T

112287242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38785957-C-T

112287671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38785651-G-A

112288199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38785288-A-G

112288275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38785191-C-T

112288802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38785010-A-T

112288823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784997-T-G

http://identifiers.org/hco/6/GRCh38#112288918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38784896-C-A

112289425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784413-C-G

112289425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784413-C-T

112289530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784311-G-A

112289567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784274-G-A

112289707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38784149-G-A

112289840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783415-A-G

112289988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783259-G-T

112290237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38783041-G-A

112290312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782965-T-C

112290355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782955-C-T

112290587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782936-C-T

112290706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782832-C-T

112290759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782794-C-T

http://identifiers.org/hco/6/GRCh38#112291134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38782423-A-C

http://identifiers.org/hco/6/GRCh38#112291247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38782276-C-A

112291276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782248-C-T

112291312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38782212-A-T

112291588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38781968-C-T

http://identifiers.org/hco/6/GRCh38#112291589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38781967-A-C

112291589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38781967-A-T

112291795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38781644-T-C

112291795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38781644-T-G

112292146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38780802-A-G

112292287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38780662-A-G

112292363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38780589-A-G

112292440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38780535-A-G

112292465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38780510-G-A

112292566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38780404-G-A

112292566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38780404-G-T

112292854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38780146-G-T

112293426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38778768-A-G

http://identifiers.org/hco/6/GRCh38#112293743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38773487-A-C

http://identifiers.org/hco/6/GRCh38#112293824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38773398-A-C

112293824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38773398-A-G

112293900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38772880-T-C

112293926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38772852-G-A

112293951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38772820-T-C

112293998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38772774-T-C

112294254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38772535-A-G

112297362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38763749-C-T

112297402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38763713-A-G

112297473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38763653-T-C

112297627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38763492-T-C

112298238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38762777-G-T

112298364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38762655-T-C

112298422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38762597-T-G

112300331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38761897-G-A

112300499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38761729-G-C

112300507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38761721-T-C

112300525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38761703-C-T

112300540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38761688-C-T

112300889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38761299-C-G

112301007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38761186-T-C

112301031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38761162-G-A

112301054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38761139-T-G

112301086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38761106-T-C

112305164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38758088-T-C

112305261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38758000-T-A

112305274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38757987-C-T

112305454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38757662-C-T

112305617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38757457-G-A

112305756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38757320-A-G

112305883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38757196-G-T

http://identifiers.org/hco/6/GRCh38#112306238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#38756259-C-A

112306238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38756259-C-T

112306245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38756252-C-T

112306251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38756246-T-A

112306268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38756229-C-T

112306269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38756228-T-C

112306510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: non coding transcript exon variant
orthologous variants: 38755995-G-T

112306520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: non coding transcript exon variant
orthologous variants: 38755986-G-A

112306520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: non coding transcript exon variant
orthologous variants: 38755986-G-T

112306678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: non coding transcript exon variant
orthologous variants: 38755853-G-T

112306680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: non coding transcript exon variant
orthologous variants: 38755851-G-C

112306680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: non coding transcript exon variant
orthologous variants: 38755851-G-T

112306762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: non coding transcript exon variant
orthologous variants: 38755772-G-A

112306762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: non coding transcript exon variant
orthologous variants: 38755772-G-T

112306864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: non coding transcript exon variant
orthologous variants: 38755488-G-A

112306994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40333
most severe consequence: non coding transcript exon variant
orthologous variants: 38755357-A-T