144170902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 40352696-G-T

144177350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40353452-G-A

144177504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40353545-G-A

http://identifiers.org/hco/5/GRCh38#144177609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40353635-C-A

144177838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40353858-A-G

144177866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40353886-T-C

144178368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40354516-A-G

144178374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40354522-T-C

144178758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40354966-C-G

144179089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40355287-A-G

144179108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40355306-G-A

144179113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40355311-G-C

144179350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40355550-C-G

144179470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40355668-C-T

144179579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40355775-G-T

144180064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40356232-C-G

144180064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40356232-C-T

144180221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40356392-C-T

144182951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40357969-G-T

144183647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40358636-T-C

http://identifiers.org/hco/5/GRCh38#144184895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40359304-A-C

144184931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40359330-T-C

144186503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40360408-G-A

144186644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40360525-A-G

144186666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40360547-C-G

144186666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40360547-C-T

144187386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40362771-G-A

144187386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40362771-G-T

144187499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40362860-C-T

144187690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40362979-C-G

144187934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40363137-C-G

144187942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40363145-C-T

144187980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40363190-C-T

144188000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40363206-C-T

144188497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40363687-C-T

144188555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40363743-G-A

http://identifiers.org/hco/5/GRCh38#144188760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40363931-A-C

144188760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40363931-A-G

144188763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40363934-G-A

144189090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40364222-C-T

144189578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40364379-A-G

http://identifiers.org/hco/5/GRCh38#144189610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40364411-A-C

144189631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40364434-T-C

144189812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40364646-C-T

144189922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40364748-C-G

144190187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40364973-C-G

144190235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40365019-A-G

144190392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40365157-C-T

144191165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40372752-G-A

http://identifiers.org/hco/5/GRCh38#144191446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40373028-C-A

144191530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40373101-T-C

144191530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40373101-T-G

144191689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40373263-G-C

144191710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40373288-G-A

144191823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40373412-T-C

144191823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40373412-T-G

144192016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40373579-C-T

144192412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40373934-T-C

http://identifiers.org/hco/5/GRCh38#144192449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40373972-A-C

http://identifiers.org/hco/5/GRCh38#144192634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40374155-C-A

144192634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40374155-C-T

144192648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40374168-C-T

144192779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40374291-C-T

http://identifiers.org/hco/5/GRCh38#144192885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40374396-C-A

144193087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40374677-G-C

144193108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40374699-C-G

144193162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40374753-C-G

144193539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40375117-C-G

http://identifiers.org/hco/5/GRCh38#144193622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40375198-C-A

144193622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40375198-C-G

144193622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40375198-C-T

144193634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40375210-G-A

144193818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40375394-A-G

144193818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40375394-A-T

144193855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40375431-T-C

144194210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40377869-G-T

144194257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40377911-G-A

http://identifiers.org/hco/5/GRCh38#144194328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40377979-C-A

144194343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40377993-G-A

144194486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40378139-C-G

http://identifiers.org/hco/5/GRCh38#144194544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40378197-C-A

144194545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40378198-A-G

144194672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40378318-G-A

144195155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40380490-C-T

144195251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40380631-C-T

http://identifiers.org/hco/5/GRCh38#144195477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40380855-C-A

144195777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40381133-T-C

144195956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40381307-C-T

http://identifiers.org/hco/5/GRCh38#144200056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40384075-C-A

144200074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40384102-G-A

144200288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40384268-A-G

144200660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40384641-C-T

144201284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40384905-T-G

144201339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40384972-T-C

144201651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40385267-G-C

144201672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40385286-G-T

144201810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40385452-A-T

http://identifiers.org/hco/5/GRCh38#144202073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40385703-C-A

144202073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40385703-C-T

144202111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40385741-C-T

144202190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40385815-G-A

144202207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40385832-G-A

144202421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40386029-G-C

144202425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40386033-T-A

144202862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40386416-A-G

144203695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40388457-T-C

http://identifiers.org/hco/5/GRCh38#144203726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40388499-C-A

144203726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40388499-C-G

144203726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40388499-C-T

144204087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40388857-G-A

144204141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40388929-T-C

144204224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40388995-A-G

144204241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40389012-G-C

144204283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40389053-T-C

144205066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40389751-C-T

144205184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40389856-A-G

144205818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 40390479-A-G

144206109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40390799-T-A

144206109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40390799-T-C

144206248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40390938-A-G

144206299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40390991-T-G

144206462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 5 prime UTR variant
orthologous variants: 40391156-T-G

144206664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 5 prime UTR variant
orthologous variants: 40391366-C-G

http://identifiers.org/hco/5/GRCh38#144206665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40391367-C-A

144206954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: synonymous variant
orthologous variants: 40391653-C-T

144207023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: missense variant
orthologous variants: 40391722-A-T

http://identifiers.org/hco/5/GRCh38#144207260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40391959-A-C

144207305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: synonymous variant
orthologous variants: 40392004-G-A

http://identifiers.org/hco/5/GRCh38#144207509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40392208-C-A

144207509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: missense variant
orthologous variants: 40392208-C-G

144207585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40392278-A-G

144207685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40392340-A-G

144208107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40392770-T-A

http://identifiers.org/hco/5/GRCh38#144208591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40393186-C-A

http://identifiers.org/hco/5/GRCh38#144208618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40393213-C-A

144208677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40393273-T-C

144208791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40393387-G-A

144209042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40393623-G-A

144209096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40393671-A-G

144209319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40393779-G-A

144209545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40393993-G-A

144209786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40394240-A-G

144209842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40394286-A-G

144209856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40394300-A-G

144209982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40394416-C-T

144210102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40394534-G-A

144210113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40394545-C-G

144210113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40394545-C-T

144210128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40394558-A-G

144210200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40394620-A-G

144210200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40394620-A-T

144210341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40394737-C-T

144210526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40394868-C-T

http://identifiers.org/hco/5/GRCh38#144210707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40395007-A-C

144210976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40395256-A-G

144211216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40395506-T-C

144212128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40396068-G-A

144212230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40396176-G-T

144212275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40396221-T-C

144212279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40396225-G-A

144212434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40396377-G-C

http://identifiers.org/hco/5/GRCh38#144212475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40396425-A-C

144212482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40396431-T-C

http://identifiers.org/hco/5/GRCh38#144212501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40396454-C-A

144212752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40396694-C-T

144212878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40396821-A-G

144212885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40396828-G-A

144212885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40396828-G-C

144213124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40397032-T-G

144213251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40397152-T-C

http://identifiers.org/hco/5/GRCh38#144213466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40397207-A-C

144213882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40397496-T-C

144213931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40397535-G-A

144213952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40397556-G-A

144214100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40397722-G-A

144214141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40397762-T-C

http://identifiers.org/hco/5/GRCh38#144214324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40397935-C-A

144214324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40397935-C-G

144214324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40397935-C-T

144214355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40397962-T-C

144215046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40398606-G-T

144215535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40399406-G-T

144216009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40399965-A-G

144216142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40400066-C-G

144216181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40400102-G-A

144216284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40400207-T-C

144216284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40400207-T-G

144216360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40400278-C-T

144216948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40400526-G-A

144217059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40400640-G-A

144217059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40400640-G-C

144217325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40400987-C-T

144217352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40401066-A-T

144217807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40401738-A-G

144217840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40401772-G-A

144217895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40401811-T-C

144218404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40402223-G-A

144218755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40402565-G-A

144219910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40403061-C-T

144219966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40403117-T-A

144220234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40403381-G-A

144220552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40403699-A-G

144220896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40403847-A-G

144220974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40403907-T-A

144220974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40403907-T-G

144221040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40403933-G-A

144224212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40405260-T-C

144224359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40405381-A-T

http://identifiers.org/hco/5/GRCh38#144224416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40405421-C-A

144224416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40405421-C-G

144224450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40405457-G-A

144224450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40405457-G-T

http://identifiers.org/hco/5/GRCh38#144224750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40405720-A-C

144224932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40405919-A-G

144224997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40405984-T-C

144225097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40406144-A-G

144225116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40406162-C-T

144225119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40406165-A-T

http://identifiers.org/hco/5/GRCh38#144225134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40406177-C-A

144225192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40406235-G-A

144225248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40406289-C-T

144225614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40406770-T-C

144225807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40406940-C-T

144226052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40407169-T-C

144226111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40407217-A-G

144226332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40407420-C-T

144226452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40407531-G-C

144227365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40408535-A-G

144227380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40408550-T-C

144227490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40408641-G-A

144227689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40408789-A-G

144227707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40408807-C-T

144228262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40409209-G-A

http://identifiers.org/hco/5/GRCh38#144228653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40409542-A-C

144228668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40409557-A-G

144228728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40409626-T-C

144228761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40409656-A-G

144228769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40409664-A-G

144229588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40411368-T-G

144229613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40411393-A-G

144230384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40411946-A-G

144230434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40411998-C-T

144230728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40412290-A-G

144230739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40412301-G-A

144231109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40412646-C-G

144231115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40412652-A-G

144231203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40412721-T-G

144231465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40413084-A-T

144231490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40413109-T-G

144232390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40414004-A-G

144232409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40414016-G-A

144232666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40414255-T-G

http://identifiers.org/hco/5/GRCh38#144232702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40414285-C-A

144232702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40414285-C-T

144232730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40414315-C-T

144232767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40414348-T-C

144232784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40414365-A-G

http://identifiers.org/hco/5/GRCh38#144232786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40414367-C-A

144232997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40417677-G-A

144232997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40417677-G-T

144233245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40417929-G-T

144233367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40418055-A-T

http://identifiers.org/hco/5/GRCh38#144233443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40418129-C-A

144233443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40418129-C-T

144233836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40418503-C-T

144234173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40418831-A-G

144234234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40418890-A-G

144234358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40419019-C-T

144234492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40419150-T-G

144234588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40419232-A-G

144234607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40419251-C-T

144234724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40419437-C-T

144234985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40419666-T-C

144235128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40419798-G-A

144235679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40420353-G-C

144235763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40420473-A-T

144235794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40420505-C-G

144235930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40420964-G-C

144235984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40421012-T-C

144236923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40421758-A-G

144237013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40422438-G-C

144237052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40422474-C-T

http://identifiers.org/hco/5/GRCh38#144237186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40422597-A-C

144237586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40422996-T-C

144237715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40423158-G-A

144237765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40423198-T-A

144237944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40423364-T-C

144238172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40423590-A-G

144238192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40423610-G-T

144238228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40423646-G-A

144238421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40423807-G-A

144238591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40423937-T-C

144238662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40424013-T-C

144238850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40424168-T-C

144238871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40424190-C-T

144239469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40424673-A-T

144240021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40425207-C-G

144240058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40425241-A-T

144240217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40425403-T-G

144240470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40425622-C-G

144240470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40425622-C-T

144240645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40425801-T-C

144240779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40425929-G-A

144240845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40425995-G-A

144241595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40426774-A-G

144241714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40426891-T-C

144241997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40427174-A-G

144242058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40427235-C-G

144242414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40427598-A-G

144242454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40427634-G-A

144244122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40431263-C-T

144244233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40431361-A-G

144244233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40431361-A-T

144244341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40431468-G-A

144244361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40431488-G-C

144244452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40431619-G-T

144244508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40431673-A-G

144244740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40432242-C-T

144244858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40432360-T-C

144245983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40433007-T-C

144245989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40433025-T-A

144245989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40433025-T-C

144246033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40433069-C-T

http://identifiers.org/hco/5/GRCh38#144246059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40433090-A-C

144246540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40433492-G-A

144246540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40433492-G-C

144246558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40433510-G-A

144246900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40433786-G-A

144246900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40433786-G-T

144247044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40433933-T-G

144247206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40434101-C-T

144248474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40436198-G-T

144249272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40437341-G-A

144249279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40437348-G-T

http://identifiers.org/hco/5/GRCh38#144249405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40437563-C-A

144249683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40437816-G-T

144249718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40437849-A-T

144249813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40437924-G-A

144249995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40438114-G-A

144250021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40438139-T-A

144250212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, missense_variant
orthologous variants: 40438346-C-T

144250280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40438411-C-T

144250365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40438484-C-T

144250485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40438599-T-A

144250485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40438599-T-C

http://identifiers.org/hco/5/GRCh38#144251044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40438946-A-C

http://identifiers.org/hco/5/GRCh38#144251135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40439725-A-C

144251422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40439945-T-A

144252481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40442795-G-T

144252640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40443308-A-T

144252755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40443431-A-G

144252755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40443431-A-T

144252789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40443464-G-A

144252938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40443608-C-G

144253160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40443808-C-T

http://identifiers.org/hco/5/GRCh38#144253198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40443845-C-A

144253616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40444237-A-G

http://identifiers.org/hco/5/GRCh38#144253648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40444287-C-A

144254418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40444977-T-C

144254732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40445154-T-C

144254732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40445154-T-G

http://identifiers.org/hco/5/GRCh38#144255582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40446003-C-A

144256060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40446451-A-T

144256080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40446483-G-T

144256093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40446496-T-A

144256093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40446496-T-G

144256717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447087-G-C

144256726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447096-G-C

144256838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447184-A-G

144256872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447231-A-G

http://identifiers.org/hco/5/GRCh38#144256879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40447238-A-C

144256879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447238-A-G

144256940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447356-C-T

144257061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447492-G-A

144257090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447524-G-A

144257090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447524-G-C

144257111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447541-G-A

144257127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447557-G-A

144257242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447648-T-C

144257266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447672-G-C

144257320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447720-C-T

144257411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447812-T-A

144257833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447926-G-C

144257884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447974-C-T

144257885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40447975-A-G

144258014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40448095-C-T

144258021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40448102-T-G

144258128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40448196-A-G

http://identifiers.org/hco/5/GRCh38#144258182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40448249-C-A

144258318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40448307-A-G

144258536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40448374-C-T

http://identifiers.org/hco/5/GRCh38#144258783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40448651-C-A

144258783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40448651-C-T

144259241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40449129-G-C

144259271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40449159-A-G

144259430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40449299-G-T

144259457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40449326-G-A

144259585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40449451-G-A

144259852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40449722-C-T

144260209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40450087-G-C

http://identifiers.org/hco/5/GRCh38#144261123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40450866-C-A

144261395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40451068-A-T

144261549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40451221-C-G

144261739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40451412-T-C

http://identifiers.org/hco/5/GRCh38#144261747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40451420-C-A

144261747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40451420-C-G

144262485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40453347-C-G

144262508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40453368-C-T

144262630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40453485-C-T

144263317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40454402-C-T

144263468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40454553-A-G

144265055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40456087-T-C

144265223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40456250-C-T

144265711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40457135-T-A

144265711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40457135-T-C

144265867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40457221-G-A

144265903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40457256-T-C

144265950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40457319-A-G

144266305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40457573-G-T

144266345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40457613-T-A

144266345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40457613-T-C

144266348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40457616-C-T

144266394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40457667-T-A

144266441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40457713-G-A

144266937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40458185-C-T

http://identifiers.org/hco/5/GRCh38#144267023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40458223-A-C

144267330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40458476-C-T

144267396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40458535-T-C

144273943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40463703-A-G

144274318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40464006-A-G

144274327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40464011-G-T

144274328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40464012-G-C

144274399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40464082-G-T

144274435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40464126-A-G

144274435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40464126-A-T

http://identifiers.org/hco/5/GRCh38#144274480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40464171-C-A

144274480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40464171-C-T

144274553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40464241-G-A

144274553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40464241-G-C

144274559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40464247-G-A

144274710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40464382-C-T

144274908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40464544-A-T

144274955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40464590-A-G

144275249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40464885-A-G

http://identifiers.org/hco/5/GRCh38#144275358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40464976-A-C

144275633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40465239-C-T

144275864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40465460-C-T

144275903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40465491-A-G

144275999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40465619-A-G

144276101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40465735-C-T

http://identifiers.org/hco/5/GRCh38#144276150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40465793-C-A

144276368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40466020-T-C

144276539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40467197-A-G

144277079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40467453-T-C

144277079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40467453-T-G

144277164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40467532-G-A

144282670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40474322-G-A

144284046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40477131-T-C

144284318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40477400-G-A

144284412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40477488-C-T

144284477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40477547-C-G

144284834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40477876-C-G

144285105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40478138-A-G

144285167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40478190-C-G

144285167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40478190-C-T

144285295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40478308-C-G

144285408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40478622-T-C

http://identifiers.org/hco/5/GRCh38#144285443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40478723-C-A

http://identifiers.org/hco/5/GRCh38#144285493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40478817-A-C

144285570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40478893-G-T

144285589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40478915-A-G

http://identifiers.org/hco/5/GRCh38#144285724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40479052-A-C

144285724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40479052-A-G

144285724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40479052-A-T

144285812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40479150-C-G

144285876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40479211-C-T

144285953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40479293-C-T

144286212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40479528-G-A

144286320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40479616-G-A

144286712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40480084-T-A

144287002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40480346-A-G

144287039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40480381-G-T

144287061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40480404-G-T

http://identifiers.org/hco/5/GRCh38#144288173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40482243-C-A

http://identifiers.org/hco/5/GRCh38#144288198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40482268-A-C

144288214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40482284-G-A

144288362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40482425-C-T

144288608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40482570-G-C

144289202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40482793-A-G

144289495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40483062-G-A

144289495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40483062-G-C

144289747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40483213-C-T

144290579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40484674-T-C

http://identifiers.org/hco/5/GRCh38#144290642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40484740-C-A

144290707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40484805-A-G

144290793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40484899-A-G

http://identifiers.org/hco/5/GRCh38#144290992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40485101-C-A

144290992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40485101-C-T

http://identifiers.org/hco/5/GRCh38#144290996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40485105-A-C

144291005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40485114-C-T

144291022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40485149-A-G

144291070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40485201-G-A

http://identifiers.org/hco/5/GRCh38#144291257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40485370-C-A

144291257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40485370-C-T

144291296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40485406-G-A

144291473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40485577-A-G

144293240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40488515-T-C

144293326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40488588-G-C

http://identifiers.org/hco/5/GRCh38#144293391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40488642-A-C

144293539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40489132-A-G

144293874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40489455-C-T

144294200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40489458-C-T

144294598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40489902-A-T

144294687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40490018-T-G

144294779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40490101-C-T

144294789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40490111-T-C

144295296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40490730-T-C

144295356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40490771-T-G

144295526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40490932-T-G

144295812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40491215-G-A

144295895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40491306-G-A

144295929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40491337-G-A

144295959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40491367-C-G

144295959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40491367-C-T

144296236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40491638-A-G

144296414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40491751-C-G

144296859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40492204-G-A

144296859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40492204-G-T

144297152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40492505-C-T

144299369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40493256-C-T

144299518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40493493-T-A

144299686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40493718-G-A

144299749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40493790-T-G

144299967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40494267-G-A

144299980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40494280-G-C

144300105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40494397-C-T

144300221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40494496-G-A

144300675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40495294-C-G

144300675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40495294-C-T

144300840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40495436-C-T

144301847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40498324-T-C

144302084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40498517-T-C

144302085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40498518-A-G

144302147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40498576-C-G

144302149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40498578-G-T

http://identifiers.org/hco/5/GRCh38#144302270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40498694-C-A

144302289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40498713-A-T

144302434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40498868-T-G

144303367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40499818-A-G

144303367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40499818-A-T

144303399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40499888-A-T

144303437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40499926-G-A

144303532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40500013-G-T

144303573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40500054-G-A

144303678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40500138-A-G

144303678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40500138-A-T

144303765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40500201-G-C

144303997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40500433-A-G

144304127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40500556-G-A

144304440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40500867-G-A

144304742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40502012-C-G

144304839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40502107-A-G

144304997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40502247-T-G

144305230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40502481-G-A

144305838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40502775-T-C

144306038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40502935-A-G

144306092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40503010-A-G

144306405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40503277-G-T

144306598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40503436-C-T

144306786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40503598-C-G

144306795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40503607-T-G

144306848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40503651-C-T

144306868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40503668-G-A

http://identifiers.org/hco/5/GRCh38#144306879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40503679-C-A

144306879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40503679-C-T

144306929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40503725-A-G

144307614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40504461-A-G

144307791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40504629-C-T

http://identifiers.org/hco/5/GRCh38#144307821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40504659-C-A

144307821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40504659-C-G

144307956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40504793-C-T

144308328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40505140-C-T

144308439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40505249-G-C

144308928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40505776-G-A

144308974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40505820-A-G

144309225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40506061-T-G

http://identifiers.org/hco/5/GRCh38#144309421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40506364-C-A

144309489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40506431-G-T

http://identifiers.org/hco/5/GRCh38#144309639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40506590-C-A

144309639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40506590-C-T

144309662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40506614-C-T

144309719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40506672-C-T

144309755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40506710-T-A

144309901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40506846-T-C

144309924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40506866-T-A

144309939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40506881-T-C

144309999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40506943-C-T

144310084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40507014-T-C

144310903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40507242-G-A

144311793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40507626-C-T

144312853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40508829-A-G

144312855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40508831-G-C

144313457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40509862-T-C

144313856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40510256-T-C

144314181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40510584-A-G

144314277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40510676-T-G

http://identifiers.org/hco/5/GRCh38#144314768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40511665-A-C

144314826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40511717-C-T

144314830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40511721-A-T

http://identifiers.org/hco/5/GRCh38#144315030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40511907-C-A

144315030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40511907-C-G

144315030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40511907-C-T

144315071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40511946-T-G

144315136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40512013-T-C

144317215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40513248-G-A

144317243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40513275-A-G

144317247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40513279-A-G

144317338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40513632-T-A

144317338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40513632-T-C

144317562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40513828-G-T

144317905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40514093-A-G

144317966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40514149-G-A

144318285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40514459-A-T

144318327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40514487-G-T

144318357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40514518-T-C

144318641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40514795-G-A

144318793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40514949-G-A

144318853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40515027-A-G

144318906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40515085-A-G

144319124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40517453-A-G

144319319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40517601-C-T

144319353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40517636-C-G

144319353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40517636-C-T

144319354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40517637-C-T

144319483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40517748-T-C

144319585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40517852-C-G

http://identifiers.org/hco/5/GRCh38#144320001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40518242-C-A

144320079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40518321-G-A

144320079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40518321-G-T

144320848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40518765-T-C

144320848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40518765-T-G

144320849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40518766-G-A

144321277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40519133-G-A

144321460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40519318-T-C

http://identifiers.org/hco/5/GRCh38#144321916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40519775-C-A

144321936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40519795-T-A

http://identifiers.org/hco/5/GRCh38#144322050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40519873-C-A

144322378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40520183-C-G

144322497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40520300-A-G

144322596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40520379-T-C

144322714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40520469-A-T

144322727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40520482-T-A

144322790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40520546-T-C

144322847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40520601-T-C

144323907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40523778-T-C

144323922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40523793-G-A

144323922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40523793-G-C

http://identifiers.org/hco/5/GRCh38#144323957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40523825-C-A

144324027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40523898-A-T

144325452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40524262-C-T

144325499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40524303-C-G

144325544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40524348-G-C

144325923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40524691-G-A

144325923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40524691-G-T

http://identifiers.org/hco/5/GRCh38#144325983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40524751-C-A

144325983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40524751-C-T

144326232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40524966-A-G

144326543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40525279-A-G

144326768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40526320-A-G

144326857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40526425-A-G

144327040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40526609-T-C

144327077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40526638-G-A

144327077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40526638-G-C

144327311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40527469-A-G

144327732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40528333-T-C

144327762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40528363-G-T

144327836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40528399-T-G

http://identifiers.org/hco/5/GRCh38#144327969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40528529-C-A

144327969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40528529-C-T

144327970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40528530-G-A

144328112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40528676-C-T

144328170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40528734-A-G

144329824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40530658-A-T

144329867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40530701-A-T

http://identifiers.org/hco/5/GRCh38#144329889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40530725-A-C

144330007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40530833-G-A

144330480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40530997-C-T

144330588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40531086-C-G

144330588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40531086-C-T

144330682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40531173-T-A

144330905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40531527-C-G

144330905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40531527-C-T

144330960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40531570-G-T

144331157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40531747-G-C

http://identifiers.org/hco/5/GRCh38#144331711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40532685-A-C

144331711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40532685-A-T

144332029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40532966-G-A

144332134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40533072-A-T

144333547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40535011-C-T

144333691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40535178-C-T

144333856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40535296-C-T

144333874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40535314-T-C

144334133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40535564-T-C

144335300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40536980-A-G

144335536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40537204-T-A

144335656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40537390-G-A

http://identifiers.org/hco/5/GRCh38#144335684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40537423-A-C

http://identifiers.org/hco/5/GRCh38#144336033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40537707-C-A

144336520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40538175-C-T

144336612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40538267-C-G

144336828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40538484-A-G

144336829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40538485-A-G

144336902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40538562-A-T

144337023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40538659-A-G

144337154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40538758-T-C

144337243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40538851-G-A

144337949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40539462-A-G

http://identifiers.org/hco/5/GRCh38#144338481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40539729-C-A

144338578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40539813-G-C

144339158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40540424-G-C

http://identifiers.org/hco/5/GRCh38#144339368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40540625-C-A

144339368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40540625-C-G

144339477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40540711-A-G

http://identifiers.org/hco/5/GRCh38#144339705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40540873-C-A

144339822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40540985-G-A

144341267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40541989-G-T

144341291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40542013-G-A

144341397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40542116-C-G

144341723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40542428-G-A

144341956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40542671-C-T

144342024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40542750-T-A

144345429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40542826-A-G

144345470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40542867-A-T

144345536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40542928-G-T

144347580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40543407-A-T

http://identifiers.org/hco/5/GRCh38#144350482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40546726-A-C

144350555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40546800-A-G

http://identifiers.org/hco/5/GRCh38#144350733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40546942-A-C

144350747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40546956-C-T

144352070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40549612-G-A

144352075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40549617-A-G

144352200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40549743-A-G

144352432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40549918-A-G

144352532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40550010-G-A

144353067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40550524-G-A

http://identifiers.org/hco/5/GRCh38#144353104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40550559-A-C

144354567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40552112-C-T

144354571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40552116-G-A

144354609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40552143-G-A

144354641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40552175-G-A

144354701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40552239-C-T

144355323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40552894-A-T

144355491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40553025-A-G

144355789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40553456-C-G

144355825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40553514-T-C

144355918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40553608-A-T

144355942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40553632-T-A

144356220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40553808-T-C

144356636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40554845-T-C

144357022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40556823-C-G

144357619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40558618-G-A

144357619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40558618-G-T

144357703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40558690-G-A

144357791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40558775-A-G

144358296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40559109-T-A

144358296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40559109-T-G

144358791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40559398-G-T

144358931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40559527-G-A

144359111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40559683-G-A

144359145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40559717-G-A

144359299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40559869-A-G

144359921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40560463-A-G

144360020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40560559-A-G

144361940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40561132-G-C

144361940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40561132-G-T

144362296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40561466-G-A

144362323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40561498-G-A

144362581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40561769-A-G

144362594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40561782-G-A

144362930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40562036-C-G

144364187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40562959-G-A

144364464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40563238-T-C

144364885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40563649-T-C

144365049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40563799-C-T

144365105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40563859-T-C

144365251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40563981-T-G

144365318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40564136-C-T

144365327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40564145-G-A

144365548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40564366-A-G

144365759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40564565-G-A

144365759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40564565-G-T

144365886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40564681-T-C

144365947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40564737-T-C

144365969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40564760-A-G

144366381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40565149-C-T

144366476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40565212-C-T

144366559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40565279-C-G

144366647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40565421-A-G

144366647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40565421-A-T

144367347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40566001-T-C

144367438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40566068-T-G

144367957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40567791-A-G

144368002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40567835-A-T

144368441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40568260-G-C

144368621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40568407-T-G

144369085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40568908-T-C

http://identifiers.org/hco/5/GRCh38#144369189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40569033-C-A

144369189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40569033-C-T

144369263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40569108-G-A

144369263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40569108-G-T

144369352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569199-G-A

144369352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569199-G-T

http://identifiers.org/hco/5/GRCh38#144369369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40569216-C-A

144369369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569216-C-G

144369460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569310-G-A

144369468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569318-C-T

144369469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569319-A-G

144369522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569370-G-A

144369522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569370-G-T

144369524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569372-A-G

144369714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569577-A-G

144369770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569632-C-G

144369887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569733-A-G

144369973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569805-G-A

144370133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569892-T-A

144370133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40569892-T-C

144370522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40570398-C-T

144370713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40570555-A-G

144371081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40570835-C-T

http://identifiers.org/hco/5/GRCh38#144371110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40570867-A-C

144371350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40571185-A-G

http://identifiers.org/hco/5/GRCh38#144371402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40571256-C-A

144371402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40571256-C-G

144371823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40571538-C-G

144371968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40571660-A-G

144372184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40571882-T-A

144372184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40571882-T-C

144372184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40571882-T-G

http://identifiers.org/hco/5/GRCh38#144372528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40572340-C-A

144372528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40572340-C-G

144373026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40572808-A-G

144373064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40572846-A-G

144373429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40573176-G-T

144375344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40576242-G-T

144375559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40576432-G-A

http://identifiers.org/hco/5/GRCh38#144375713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40576553-C-A

144377130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40577674-G-A

144377210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40577748-G-A

144377243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40577780-C-G

144377271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40577810-A-G

144377278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40577817-A-G

144377309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40577842-A-G

http://identifiers.org/hco/5/GRCh38#144377330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40577864-C-A

http://identifiers.org/hco/5/GRCh38#144377459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40577995-A-C

144377613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40578302-T-C

144377640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40578329-T-C

144377692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40578382-A-T

144377697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40578387-G-A

144377719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40578409-G-T

http://identifiers.org/hco/5/GRCh38#144377740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40578430-C-A

144377760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40578450-A-G

144377780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40578470-A-G

144377809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40578498-C-G

http://identifiers.org/hco/5/GRCh38#144377863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40578554-C-A

http://identifiers.org/hco/5/GRCh38#144377865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40578556-A-C

144377865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40578556-A-G

144377935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40578623-C-T

144377953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40578641-G-A

http://identifiers.org/hco/5/GRCh38#144378014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40578786-A-C

144378014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40578786-A-G

144378329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40579100-A-G

144378962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40579666-T-C

144378966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40579670-G-A

144378966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40579670-G-C

144379085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40579778-T-C

144379521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40580183-A-G

144379538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40580200-C-G

144379640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40580287-G-A

144379640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40580287-G-T

144379724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40580385-A-G

144379724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40580385-A-T

144379887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40580694-T-C

144379982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40580800-C-T

144382727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40581892-G-C

144382860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40582030-A-G

144382920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40582089-A-G

http://identifiers.org/hco/5/GRCh38#144382956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40582125-C-A

144382985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40582153-C-T

144383021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40582186-T-C

144383072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40582222-G-T

http://identifiers.org/hco/5/GRCh38#144383203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40582412-A-C

144383229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40582512-T-C

144383263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40582546-A-T

144383273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40582556-T-A

http://identifiers.org/hco/5/GRCh38#144383281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40582565-C-A

http://identifiers.org/hco/5/GRCh38#144383339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40582623-C-A

144383366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40582650-C-G

144383367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40582651-T-A

http://identifiers.org/hco/5/GRCh38#144383620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40582907-C-A

144383620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40582907-C-T

144383672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40582956-C-G

144383672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40582956-C-T

144384014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40583906-G-T

144384065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40583956-T-C

144384182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40584077-A-G

144384224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40584118-A-G

144384226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40584120-A-G

144384263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40584158-G-T

144384301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40584186-G-C

144384316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40584201-G-T

144384333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40584218-A-G

http://identifiers.org/hco/5/GRCh38#144384448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40584330-C-A

144384448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40584330-C-G

144384448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40584330-C-T

144384739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40584551-A-G

144384752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40584564-T-C

144384769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40584581-A-G

144384868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40584744-G-A

144384869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40584745-T-C

144385200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40585062-C-T

144385311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40585146-G-T

144385432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40585267-C-T

144385775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40585547-T-C

144385789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40585561-G-C

144385798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40585570-T-A

144385844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40585611-C-G

144385923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40585702-T-C

http://identifiers.org/hco/5/GRCh38#144386051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40585967-A-C

144386052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40585968-G-T

144386183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40586099-A-G

144386535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40586452-G-C

144386654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40586558-T-C

144386723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40586629-A-T

144386730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40586636-A-G

144386809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40586690-C-T

144386905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40586790-G-A

144386905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40586790-G-C

144386918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40586803-C-T

144388021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40587045-A-T

http://identifiers.org/hco/5/GRCh38#144388030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40587054-C-A

144388030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40587054-C-T

144388842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40587550-C-T

144389070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40587773-C-T

144390093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40588227-T-A

144390093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40588227-T-G

http://identifiers.org/hco/5/GRCh38#144390177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40588312-C-A

144390336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40588465-G-A

144390372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40588505-G-T

144390443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40588580-G-A

144390970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40588752-T-C

144390998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40588780-G-A

144391010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40588792-C-G

144391203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40588965-A-G

144391947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40589706-A-G

144392248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40589951-T-C

http://identifiers.org/hco/5/GRCh38#144392529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40590176-A-C

144392529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40590176-A-G

144392572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40590219-C-T

144393980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40592042-T-C

144393980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40592042-T-G

144394007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40592085-G-T

144394011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40592089-A-T

144394161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40592239-C-G

144394370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40592441-G-A

144394453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40592511-C-T

144394478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40592535-C-G

http://identifiers.org/hco/5/GRCh38#144395066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40598913-C-A

http://identifiers.org/hco/5/GRCh38#144395349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40599185-C-A

144395458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40599287-A-G

http://identifiers.org/hco/5/GRCh38#144395485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40599314-C-A

144395485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40599314-C-G

144395567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40599382-T-C

http://identifiers.org/hco/5/GRCh38#144395670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40599485-C-A

144395759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40599574-G-A

144395788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40599603-G-C

144396108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40599953-A-G

144396227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40600110-G-A

144396285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40600168-C-T

144396360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40600252-C-G

http://identifiers.org/hco/5/GRCh38#144396445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40600322-A-C

144396546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40600418-C-T

http://identifiers.org/hco/5/GRCh38#144396634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40600496-A-C

http://identifiers.org/hco/5/GRCh38#144398132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40600789-A-C

144398166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40600823-G-T

144398250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40600924-A-G

144398273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40600947-T-C

144398436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40601107-T-C

144398574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40601241-T-C

144398576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40601243-C-T

144398595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40601270-T-G

144398716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40601399-T-G

http://identifiers.org/hco/5/GRCh38#144398822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40601499-C-A

144398822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40601499-C-T

http://identifiers.org/hco/5/GRCh38#144399787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40602427-C-A

144399890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40602528-G-C

144400390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40602971-A-G

144400530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40603100-G-A

144400668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40603201-C-G

144400750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40603290-A-G

144400882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40603499-G-C

http://identifiers.org/hco/5/GRCh38#144400919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40603534-A-C

144400919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40603534-A-T

144401828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40604739-A-G

http://identifiers.org/hco/5/GRCh38#144402389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40605191-C-A

144403118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40605531-C-G

144403493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40605864-G-A

144403866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40606122-T-C

144404051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40606252-C-T

144404476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40606657-C-T

144404615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40606805-A-G

144404615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40606805-A-T

144404742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40606921-G-C

http://identifiers.org/hco/5/GRCh38#144405496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40607644-C-A

http://identifiers.org/hco/5/GRCh38#144405521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40607669-C-A

144405603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40607752-A-G

http://identifiers.org/hco/5/GRCh38#144405697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40607851-C-A

144405697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40607851-C-T

144405959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40608110-C-G

144406004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40608160-G-A

144406233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40608914-G-T

144406378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40609052-A-G

144406533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40609197-T-C

144406568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40609231-T-C

144406579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40609242-G-A

144406679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40609315-A-G

144406821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40609458-C-T

144407041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40609692-G-A

144410243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40610057-C-T

144413649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40611647-C-T

144413801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40611791-G-A

144413903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40611900-G-T

144413906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40611903-T-A

http://identifiers.org/hco/5/GRCh38#144413952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40611943-C-A

144414491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40612504-G-T

144414626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40612634-G-A

144414661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40612668-T-C

144414863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40612870-G-A

http://identifiers.org/hco/5/GRCh38#144415630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40613182-A-C

144415695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40613251-T-C

144415759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40613309-T-C

144420965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40615921-G-A

144421024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40615981-C-T

144421157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40616120-T-C

144421521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40616493-A-G

144421521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40616493-A-T

144421531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40616503-T-C

144421531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40616503-T-G

144421565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40616537-G-C

144421590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40616559-T-G

http://identifiers.org/hco/5/GRCh38#144421597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40616566-A-C

http://identifiers.org/hco/5/GRCh38#144421887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40617248-C-A

http://identifiers.org/hco/5/GRCh38#144421935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40617294-A-C

144422126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40617984-A-G

http://identifiers.org/hco/5/GRCh38#144422259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40618118-C-A

144422326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40618185-G-T

144422330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40618189-T-G

http://identifiers.org/hco/5/GRCh38#144422479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40618336-A-C

144422533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40618390-T-C

144422608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40618460-T-C

144422914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40618767-A-G

144423227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40619052-G-A

144423227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40619052-G-T

http://identifiers.org/hco/5/GRCh38#144423377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40619156-A-C

http://identifiers.org/hco/5/GRCh38#144423487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40619274-A-C

144423575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40619315-A-G

144427114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40620533-T-C

144427114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40620533-T-G

144427396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40620809-C-T

144427398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40620811-C-T

144427401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40620814-G-A

144427472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40620879-C-G

144427731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40621125-A-G

144427731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40621125-A-T

144427773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40621167-G-A

144428262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40621356-T-G

144428297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40621391-C-G

144428999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40622083-T-C

http://identifiers.org/hco/5/GRCh38#144429034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40622121-C-A

144429034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40622121-C-G

144429095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40622183-G-T

144429171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40622264-C-G

144429171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40622264-C-T

144429340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40622434-G-A

144429340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40622434-G-T

http://identifiers.org/hco/5/GRCh38#144429608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40622674-C-A

144429608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40622674-C-T

http://identifiers.org/hco/5/GRCh38#144429660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40622733-A-C

http://identifiers.org/hco/5/GRCh38#144429788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40622841-A-C

144429860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40622909-G-A

144429907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40624213-A-T

http://identifiers.org/hco/5/GRCh38#144430125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40624397-C-A

144430125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40624397-C-T

144430136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40624408-A-G

144430374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40624640-G-T

144430768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40624915-G-A

144430859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40625003-C-T

http://identifiers.org/hco/5/GRCh38#144431054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40625396-A-C

144431054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40625396-A-G

144431396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40625715-G-A

144431677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40625967-G-C

144432017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40626354-G-C

144432119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40626455-T-C

144432121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40626457-C-T

144433663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40629635-C-T

144434215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40630183-G-A

144434215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40630183-G-C

144434464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40630420-A-G

144434513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40630467-G-A

144434539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40630493-A-T

144435054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40630987-G-A

144435572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40631752-G-A

144435670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40631866-A-G

144436046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40632114-A-G

144436079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40632147-G-A

http://identifiers.org/hco/5/GRCh38#144437416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#40632517-C-A

144437652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40632725-C-T

144437664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40632737-G-A

144437697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40632770-A-G

144437698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40632771-T-C

144437866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40632922-G-T

144437935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40633014-T-A

144438041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron variant
orthologous variants: 40633104-A-G

144448298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40639592-T-C

144448318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40639612-G-A

http://identifiers.org/hco/5/GRCh38#144448396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40639691-C-A

144448533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40639799-G-A

http://identifiers.org/hco/5/GRCh38#144448551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40639817-A-C

144448596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40639862-G-C

144448990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40640251-T-A

144449074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40640334-T-C

144449160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40640408-G-T

144451082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40642894-T-C

144451298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40643123-T-G

144451824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40643619-C-G

144457180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40644974-A-G

144457180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40644974-A-T

144457193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40644987-G-C

http://identifiers.org/hco/5/GRCh38#144457222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#40645016-C-A

144457409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40645415-A-G

144457419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40645445-A-G

144457462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40645488-T-A

144457479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40645520-T-C

144457617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40645747-C-T

144457703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40645837-T-G

144457761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40645898-A-G

144457878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40645976-C-T

144458762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40647870-C-T

144458809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40647917-A-G

144458944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40648053-G-C

144459107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40648217-G-A

144459245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40648417-C-T

144461018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40649190-G-C

144461079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40649243-G-T

144461484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40649640-T-G

144461501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40649657-T-G

144462021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40650019-G-C

144462065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40650065-C-G

144462065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40650065-C-T

144462198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29244
most severe consequence: intron_variant, undefined
orthologous variants: 40650214-G-A