5143185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69796644-G-A

5143210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69796620-C-T

5143256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69796590-C-T

5143354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69796508-A-G

5143461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69796417-C-T

5143471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69796407-C-T

5143617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69796283-A-G

5144085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69795825-C-T

5144093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69795817-C-T

5144258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69795649-A-G

5144268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69795639-C-T

5144302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69795601-A-G

http://identifiers.org/hco/18/GRCh38#5144593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69795281-C-A

5144812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69795054-T-A

5144896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794990-T-C

5144918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794968-A-G

5144938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794949-A-G

5145043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794850-T-C

5145054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794839-T-A

5145132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794756-C-T

5145164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794726-A-G

5145164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794726-A-T

http://identifiers.org/hco/18/GRCh38#5145175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69794715-A-C

5145175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794715-A-G

5145175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794715-A-T

http://identifiers.org/hco/18/GRCh38#5145299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69794598-A-C

http://identifiers.org/hco/18/GRCh38#5145347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69794551-C-A

5145347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794551-C-G

5145392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794510-A-G

5145392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794510-A-T

5145418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794484-T-G

5145463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794441-G-A

5145463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794441-G-T

5145559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 3 prime UTR variant
orthologous variants: 69794343-A-G

5145592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: synonymous variant
orthologous variants: 69794310-C-T

5145794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69794109-A-G

5145816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69794082-G-T

5145851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69794056-A-G

5145857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69794050-T-A

5149297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69788465-A-G

5149397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69788376-G-A

5150281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69787776-A-G

5150374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69787682-T-C

5150856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69786757-T-G

5150952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69786660-G-A

5151005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69786602-A-G

5151217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69786386-A-T

5151398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69786211-C-T

5151697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69785939-G-C

5151810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69785832-A-G

5152628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69785144-C-T

5152724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69785063-G-C

5152746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69785041-G-T

5152778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69785015-C-T

5152863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69784930-A-G

5152896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69784892-G-A

5154344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69782969-C-T

5156798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69781197-A-G

5156836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69781162-G-A

5156885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69781116-G-A

5157058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69780962-T-G

5157202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69779980-C-T

5157288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69779900-G-T

http://identifiers.org/hco/18/GRCh38#5157388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69779769-A-C

5157515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69779654-A-G

5158062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69779481-C-T

5158186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69779331-A-G

5158440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69779102-T-C

5158798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69778692-A-G

5158814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69778676-A-G

5158839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69778651-G-A

5158889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69778604-A-G

5158932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69778561-A-T

5158944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69778550-G-A

http://identifiers.org/hco/18/GRCh38#5159001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69778505-C-A

5159025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69778470-T-C

5159153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69778322-A-G

5159199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69778278-A-G

5159203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69778274-G-A

http://identifiers.org/hco/18/GRCh38#5159257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69778223-C-A

5159257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69778223-C-T

http://identifiers.org/hco/18/GRCh38#5159328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69778168-C-A

5159328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69778168-C-T

5159334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69778162-T-C

http://identifiers.org/hco/18/GRCh38#5159536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#69777973-C-A

5159552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69777960-A-T

5159747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69777751-T-C

5159753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69777745-G-A

5159811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69777696-G-A

5163225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69777164-T-C

5163327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69777062-G-A

5163357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69777035-T-C

5163438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69776966-C-T

5163563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69776837-G-T

5163805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 69775928-G-A

5163805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 69775928-G-T

5164342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69775376-C-T

5164499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69775243-T-C

5164625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69775120-C-G

5164651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69775094-T-C

5165257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69773461-A-G

5165267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69773451-A-G

5165358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69773361-G-A

5165393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69773324-C-G

5165393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69773324-C-T

5165544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69772369-G-A

5165544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69772369-G-T

5165581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69772340-G-A

5165658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69772279-G-A

5166104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69771893-A-G

5166263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69771752-G-A

5166300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69771718-G-A

5166406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69771609-G-T

http://identifiers.org/hco/18/GRCh38#5166526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#69771507-C-A

5166526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69771507-C-G

5166571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69771465-G-C

http://identifiers.org/hco/18/GRCh38#5166926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#69771357-C-A

5166977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69771293-A-G

5167086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69770676-T-C

5167172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69770614-T-C

5167216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69770567-T-G

5167465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69770313-A-G

5167560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69770203-C-G

5167561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69770202-T-C

5167622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69770138-G-A

5167739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69770009-G-A

http://identifiers.org/hco/18/GRCh38#5168000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#69769705-C-A

5168000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69769705-C-T

5168021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69769684-A-G

5168939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69769101-A-G

5169043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69769022-T-C

5169175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69768898-T-C

5169246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69768828-G-C

5169609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69768497-C-T

5169616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69768490-T-A

http://identifiers.org/hco/18/GRCh38#5170294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#69767769-C-A

5170579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69767464-G-C

5170579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69767464-G-T

5170609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69767434-A-G

5170609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69767434-A-T

http://identifiers.org/hco/18/GRCh38#5170985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#69767106-C-A

5170985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69767106-C-T

5171086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69767000-T-A

http://identifiers.org/hco/18/GRCh38#5171104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69766982-C-A

5172530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69766774-A-G

http://identifiers.org/hco/18/GRCh38#5172658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69766632-A-C

5177169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69765997-A-G

5177212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69765956-T-C

http://identifiers.org/hco/18/GRCh38#5177222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69765946-C-A

5177222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69765946-C-T

5177383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69765797-C-T

5177439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69765758-G-A

5177472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69765720-A-G

5177484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69765699-T-A

5177720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69765498-A-G

5177828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69765401-A-G

5178020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69765238-G-A

http://identifiers.org/hco/18/GRCh38#5178096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69765172-A-C

5178415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69764568-A-G

http://identifiers.org/hco/18/GRCh38#5178665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69764361-C-A

5178803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69764254-G-A

5178814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69764243-C-G

5179037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69763140-A-G

5179038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69763139-C-T

5179057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69763122-T-G

5179058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69763121-T-A

5179753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69763027-C-T

5179892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69762831-G-A

http://identifiers.org/hco/18/GRCh38#5180324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69762378-C-A

5180407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69762311-C-T

5180673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69762061-C-G

5180718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69762018-A-G

5181385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69761534-C-T

5181534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69761391-C-G

5181560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69761362-C-T

5181647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69761296-C-G

5181736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69761221-T-C

5181814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69761137-T-C

5181894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69761030-G-T

5182312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69760686-T-C

5182334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69760665-A-T

5182458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69760016-T-C

5182550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69759923-C-T

5182583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69759889-T-G

5182645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69759846-C-T

http://identifiers.org/hco/18/GRCh38#5182692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69759801-C-A

5182692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69759801-C-T

5182814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69759698-T-A

5183049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69759370-T-C

5183119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69759216-C-T

5183122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69759213-T-G

5183224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69759111-G-T

5183242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69759093-A-G

5183262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69759041-G-A

http://identifiers.org/hco/18/GRCh38#5183592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69758738-C-A

5192534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69750945-G-A

5192691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69750805-C-T

5192708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69750789-G-T

5192838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69750669-G-A

5192897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69750603-A-G

http://identifiers.org/hco/18/GRCh38#5193177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69750346-C-A

5193177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69750346-C-G

5193177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69750346-C-T

5193886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69749720-C-G

5193886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69749720-C-T

5193887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69749719-T-A

5193938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69749668-T-C

5194088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69749530-A-T

http://identifiers.org/hco/18/GRCh38#5194137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69749485-C-A

5194137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69749485-C-T

http://identifiers.org/hco/18/GRCh38#5194165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69749460-A-C

5194173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69749452-T-C

5194476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69749143-G-A

5194514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69749084-T-C

5194558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69749053-T-C

http://identifiers.org/hco/18/GRCh38#5194591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69749025-A-C

5194862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69748824-A-G

http://identifiers.org/hco/18/GRCh38#5195128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69748626-C-A

http://identifiers.org/hco/18/GRCh38#5195130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69748624-C-A

5195136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69748618-T-C

5195159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69748603-T-A

5195577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69748225-A-G

5195952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69747745-G-C

5195952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69747745-G-T

5195955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69747742-G-A

5196003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69747684-A-G

5196009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69747678-G-T

http://identifiers.org/hco/18/GRCh38#5196405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69747110-C-A

5196871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69746687-G-A

5196897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69746673-T-A

5196897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69746673-T-C

http://identifiers.org/hco/18/GRCh38#5196933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69746640-C-A

5196933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69746640-C-G

5196933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69746640-C-T

http://identifiers.org/hco/18/GRCh38#5196945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69746628-C-A

5196945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69746628-C-G

5196945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69746628-C-T

5196970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69746601-C-T

5196974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69746597-T-A

5196974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron variant
orthologous variants: 69746597-T-C

5197043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, missense_variant
orthologous variants: 69746529-G-A

5197080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69746492-G-A

5197080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69746492-G-C

5197084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69746488-A-G

http://identifiers.org/hco/18/GRCh38#5197097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#69746475-A-C

5197097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69746475-A-G

5197114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69746456-G-A

5197159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69746410-G-T

http://identifiers.org/hco/18/GRCh38#5197199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#69746375-C-A

5197201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 69746373-G-T

5197265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69746314-C-G

5197315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69746265-T-C

http://identifiers.org/hco/18/GRCh38#5197326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#69746254-C-A

5197359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69746226-G-A

5197359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28285
most severe consequence: intron_variant, undefined
orthologous variants: 69746226-G-T