http://identifiers.org/hco/1/GRCh38#109249555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108323323-C-A

109249559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 5 prime UTR variant
orthologous variants: 108323319-G-A

109249559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 5 prime UTR variant
orthologous variants: 108323319-G-C

109249593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 5 prime UTR variant
orthologous variants: 108323285-C-T

http://identifiers.org/hco/1/GRCh38#109249751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108323131-A-C

http://identifiers.org/hco/1/GRCh38#109249979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#108322906-C-A

109250552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108322336-C-T

http://identifiers.org/hco/1/GRCh38#109251074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108321814-C-A

109251074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108321814-C-T

109251133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108321755-C-G

109251133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108321755-C-T

http://identifiers.org/hco/1/GRCh38#109251139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108321749-C-A

109251184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108321704-G-T

109251262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108321626-A-G

109251382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108321506-C-T

109251460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108321428-C-T

109251571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108321317-A-G

http://identifiers.org/hco/1/GRCh38#109251910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108320978-A-C

109251928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108320960-G-A

109251928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108320960-G-C

109251946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108320942-G-A

109251979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108320909-G-C

http://identifiers.org/hco/1/GRCh38#109252024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108320864-A-C

109252024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108320864-A-G

http://identifiers.org/hco/1/GRCh38#109252096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108320792-C-A

109252282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108320606-A-G

109252453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108320435-A-G

109252456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108320432-C-T

109252726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108320162-A-G

http://identifiers.org/hco/1/GRCh38#109252996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108319892-A-C

109252996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108319892-A-G

109252996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108319892-A-T

http://identifiers.org/hco/1/GRCh38#109253427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108319461-C-A

109253427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108319461-C-T

109253448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108319440-G-T

109253540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108319347-T-G

109253890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108318988-G-C

109253932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108318946-G-A

109253941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108318937-G-A

109254091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108318786-T-C

109254599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108318315-G-T

109254827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, undefined
orthologous variants: 108318158-C-T

109255460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108317545-T-C

109255877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108317173-G-T

109256259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108316889-C-T

109256633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108316636-C-G

109257713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108316010-C-T

109257762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108315961-T-C

109257810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108315914-C-T

http://identifiers.org/hco/1/GRCh38#109257964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108315782-C-A

http://identifiers.org/hco/1/GRCh38#109258397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108314748-C-A

109258397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108314748-C-G

109258397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108314748-C-T

109258404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108314741-T-G

109258446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108314697-G-A

109258461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108314682-G-A

109258461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108314682-G-T

http://identifiers.org/hco/1/GRCh38#109258632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108314511-C-A

109258632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108314511-C-T

109259002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108314141-C-G

109259002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108314141-C-T

109259063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: stop gained
orthologous variants: 108314080-T-A

109259063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: synonymous variant
orthologous variants: 108314080-T-C

109259509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108313612-G-C

109260107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108313170-G-A

109260107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108313170-G-C

109260177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108313075-G-T

109260309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108312956-A-G

109260350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108312919-C-T

109260654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108312639-G-A

109260735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108312609-A-G

http://identifiers.org/hco/1/GRCh38#109260946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108312421-C-A

109260946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108312421-C-T

109261233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108311694-C-T

109261239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108311688-C-T

109261271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 108311654-G-A

109261271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 108311654-G-C

109261283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108311642-G-A

109261293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108311632-G-A

109261293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108311632-G-C

109261293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108311632-G-T

http://identifiers.org/hco/1/GRCh38#109261298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108311630-C-A

109261298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108311630-C-T

109261436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108311418-G-A

109261436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108311418-G-T

109261462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108311380-G-A

109261464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108311378-A-G

http://identifiers.org/hco/1/GRCh38#109261637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108311202-A-C

109261721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108311116-C-G

http://identifiers.org/hco/1/GRCh38#109261732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108311105-C-A

109261746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108311088-C-T

109261918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310914-G-T

109261940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310890-T-A

109261940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310890-T-C

109261980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310852-T-C

109262042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310800-T-A

http://identifiers.org/hco/1/GRCh38#109262210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108310739-C-A

109262210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310739-C-G

109262210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310739-C-T

109262257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310712-T-A

109262257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310712-T-C

http://identifiers.org/hco/1/GRCh38#109262395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108310584-C-A

109262395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: synonymous variant
orthologous variants: 108310584-C-T

109262501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310471-G-A

109262608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310378-G-A

109262693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310295-G-T

109262699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310289-T-A

109262699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310289-T-C

109262751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108310230-G-A

109263019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108309968-G-A

109263019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108309968-G-C

109263064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108309928-G-A

109263395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, undefined
orthologous variants: 108309631-A-G

109263460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108309565-G-A

109263460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108309565-G-T

109263461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108309564-G-A

109263461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108309564-G-T

109263462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108309563-G-A

http://identifiers.org/hco/1/GRCh38#109263530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#108309479-C-A

109263530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, undefined
orthologous variants: 108309479-C-G

109263530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, undefined
orthologous variants: 108309479-C-T

109263532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, undefined
orthologous variants: 108309477-G-T

109263802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, undefined
orthologous variants: 108309219-C-T

109263816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, undefined
orthologous variants: 108309207-A-G

109263905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, undefined
orthologous variants: 108309127-T-A

109264037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108309035-A-T

109264125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: synonymous variant
orthologous variants: 108308954-G-A

109264324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108308755-C-T

http://identifiers.org/hco/1/GRCh38#109264388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108308691-C-A

109264388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108308691-C-G

109264646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108308438-G-A

http://identifiers.org/hco/1/GRCh38#109264648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108308436-C-A

109264769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108308330-G-A

109264772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108308327-A-G

109264785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108308312-G-A

109264815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108308284-A-G

109264924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108308177-T-G

http://identifiers.org/hco/1/GRCh38#109264954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108308147-C-A

109264954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108308147-C-T

109265080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108308052-C-T

109265103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108308029-G-A

109265106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108308026-A-G

http://identifiers.org/hco/1/GRCh38#109265165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108307963-A-C

109265358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307764-C-T

109265376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307746-A-G

109265394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307728-A-G

109265394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307728-A-T

109265405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307715-T-C

109265405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307715-T-G

109265410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307710-A-G

109265410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307710-A-T

109265449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307671-G-A

109265449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307671-G-C

109265449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307671-G-T

109265534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307584-G-C

109265640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307477-G-A

109265640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307477-G-T

http://identifiers.org/hco/1/GRCh38#109265699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108307417-C-A

109265699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307417-C-G

109265699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307417-C-T

109265711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307404-C-T

109265825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108307289-G-A

109265837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108307277-C-G

109265954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307161-C-T

109265965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307150-G-T

109265992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307124-G-A

109265992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307124-G-C

109266025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307098-G-A

109266051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108307072-G-T

109266164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108306973-T-C

109266283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108306853-G-A

109266283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108306853-G-T

http://identifiers.org/hco/1/GRCh38#109266368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108306766-C-A

109266368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108306766-C-T

109267058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108306713-G-A

109267058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108306713-G-T

109267074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108306698-A-G

109267186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108306580-G-A

109267405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108306388-T-C

109267405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108306388-T-G

109267455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108306346-T-C

109267520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108306315-G-C

109267527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108306308-C-G

109267598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108306237-C-T

109267680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108306180-T-G

http://identifiers.org/hco/1/GRCh38#109267682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108306178-C-A

109267682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108306178-C-T

109267740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108306127-A-G

109267740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108306127-A-T

http://identifiers.org/hco/1/GRCh38#109267765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108306101-C-A

109267791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108306067-A-G

http://identifiers.org/hco/1/GRCh38#109268016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108305827-C-A

109268016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108305827-C-T

109268046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108305797-G-A

109268107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108305751-G-A

109268133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108305725-G-T

109268355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108305475-G-A

109268355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108305475-G-T

109268421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108305405-G-A

109268822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108305008-G-A

109268822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108305008-G-T

http://identifiers.org/hco/1/GRCh38#109269100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108304734-C-A

http://identifiers.org/hco/1/GRCh38#109269130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108304704-C-A

109269130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108304704-C-G

109269322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108304530-G-A

109269324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108304528-A-G

109269328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108304524-G-A

109269328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108304524-G-T

109269380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108304468-A-G

109269380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108304468-A-T

109269467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108304385-A-T

109269494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense variant
orthologous variants: 108304358-C-T

109269605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108304247-G-A

109269605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108304247-G-T

109269659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron variant
orthologous variants: 108304193-C-G

109269804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108304049-A-G

109269836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108304018-G-T

109270207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108303660-T-C

109270222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108303644-A-T

http://identifiers.org/hco/1/GRCh38#109270298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108303559-C-A

109270298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108303559-C-T

109270321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108303536-G-A

109270321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108303536-G-T

http://identifiers.org/hco/1/GRCh38#109270339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108303518-C-A

109270339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108303518-C-T

109270401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108303470-G-T

http://identifiers.org/hco/1/GRCh38#109270404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108303467-C-A

109270404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108303467-C-T

109270558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108303299-T-C

109270643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108303206-G-T

109270676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108303173-T-A

109270676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108303173-T-C

http://identifiers.org/hco/1/GRCh38#109270785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108303102-C-A

109270785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108303102-C-T

109270788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108303099-G-T

http://identifiers.org/hco/1/GRCh38#109270892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108303016-C-A

109270929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 108302984-C-G

109270947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108302966-C-G

109270947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108302966-C-T

109271045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108302868-T-A

109271054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108302858-G-T

http://identifiers.org/hco/1/GRCh38#109271124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108302818-C-A

109271124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108302818-C-T

109271241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108302697-G-A

109271322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108302619-G-A

109271328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108302613-G-A

109271369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108302573-C-T

109271387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 108302555-T-C

109271411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108302531-G-A

109271529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108302393-G-A

109271570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108302348-C-T

109271660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108302261-C-T

109271669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108302252-A-G

109271809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108302129-T-C

109272080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108301852-C-T

109272218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108301716-T-C

http://identifiers.org/hco/1/GRCh38#109272412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108301520-C-A

109272419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108301513-A-T

109272447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108301487-C-T

109272454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108301480-A-G

109272517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108301416-G-A

109272555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108301378-G-T

109272658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108301320-C-T

109272789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108301190-G-A

109273069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108300921-G-A

109273177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108300813-G-C

109273198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108300792-C-T

http://identifiers.org/hco/1/GRCh38#109273350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108300639-C-A

109273459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108300536-C-T

109273465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108300530-A-G

109273465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108300530-A-T

109273552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108300443-G-A

109273552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108300443-G-C

109273552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 108300443-G-T

http://identifiers.org/hco/1/GRCh38#109273567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108300428-C-A

109273567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108300428-C-G

109273567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108300428-C-T

http://identifiers.org/hco/1/GRCh38#109273576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108300419-C-A

109273576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108300419-C-T

109273642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108300353-A-G

109273642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108300353-A-T

109273747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108300231-T-C

109273885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108300108-T-C

http://identifiers.org/hco/1/GRCh38#109274289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108299716-A-C

109274383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299612-G-A

109274383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299612-G-T

http://identifiers.org/hco/1/GRCh38#109274434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108299560-A-C

109274434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299560-A-G

109274435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299559-T-A

109274435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299559-T-G

109274491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299505-T-G

http://identifiers.org/hco/1/GRCh38#109274552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108299444-C-A

109274552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299444-C-T

109274618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299345-G-T

109274723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299242-A-G

http://identifiers.org/hco/1/GRCh38#109274765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108299197-C-A

109274765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299197-C-T

109274870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299094-G-A

109274870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299094-G-T

109274875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299089-G-A

109274875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299089-G-C

109274875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299089-G-T

109274924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299046-G-C

109274924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299046-G-T

109274929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299037-A-G

109274929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299037-A-T

109274963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108299003-T-C

109275245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108298699-G-T

109275255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108298689-T-C

109275260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108298684-A-T

109275390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108298574-A-G

109275484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108298482-T-C

http://identifiers.org/hco/1/GRCh38#109275491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108298475-C-A

109275491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108298475-C-T

109275506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108298460-C-T

http://identifiers.org/hco/1/GRCh38#109275521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3231
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108298445-C-A