http://identifiers.org/hco/4/GRCh38#52873152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74366147-C-A

52873152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: 74366147-C-G

52873152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: 74366147-C-T

52873231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: 74366226-T-C

52873342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: 74366343-G-A

52873342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: 74366343-G-T

52873426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: 74366432-C-T

http://identifiers.org/hco/4/GRCh38#52873515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74366519-C-A

52873515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: 74366519-C-T

52873543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: 74366547-T-A

52873543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: 74366547-T-C

52873610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: 74366612-G-A

52873724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: 74366722-T-A

52873724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: 74366722-T-C

52873725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3 prime UTR variant
orthologous variants: 74366723-G-T

52873925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 74366923-T-A

52874029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: synonymous_variant, undefined
orthologous variants: 74367024-T-A

52874056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: synonymous_variant, undefined
orthologous variants: 74367051-G-A

52874056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: missense_variant, undefined
orthologous variants: 74367051-G-C

52874155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74367123-T-C

http://identifiers.org/hco/4/GRCh38#52875340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74367347-C-A

52875340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74367347-C-G

52875340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74367347-C-T

52875847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74367820-T-G

http://identifiers.org/hco/4/GRCh38#52875871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74367844-A-C

52875871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74367844-A-T

52875975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74367950-C-G

52877250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74368806-G-C

52877290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74368845-G-C

52877290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74368845-G-T

52877424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74368968-T-G

52877633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74369142-G-A

52877805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74369262-C-T

http://identifiers.org/hco/4/GRCh38#52877809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74369266-A-C

52877954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74369410-T-C

52878146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74369588-C-T

52878374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74369813-G-A

52878737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74370385-C-T

52879026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74370575-T-C

52879188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74370720-A-G

52879250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74370754-T-C

52879719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74370885-C-T

52879798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74370934-G-A

52879798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74370934-G-C

52879856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74370993-G-A

http://identifiers.org/hco/4/GRCh38#52879857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74370994-C-A

52882936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74371017-T-C

52883079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74371136-G-A

52883195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74371236-C-G

52883243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74371269-G-A

52883471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74371482-T-C

52883668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74371672-C-G

52883668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74371672-C-T

52883985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74371961-C-T

52884268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74372215-T-A

52885602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74372788-G-A

52885602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74372788-G-T

52885612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74372798-G-T

52885840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: synonymous variant
orthologous variants: 74373005-G-A

52885840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: stop gained
orthologous variants: 74373005-G-C

52885840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: stop gained
orthologous variants: 74373005-G-T

http://identifiers.org/hco/4/GRCh38#52886886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74373269-C-A

52887013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74373360-T-C

52887287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74373595-T-C

http://identifiers.org/hco/4/GRCh38#52887560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74373824-A-C

52887609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74373870-T-C

52890077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74375361-T-C

52890194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74375479-A-G

52890243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74375528-G-A

52890342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74375754-G-A

52890342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74375754-G-C

52890556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74375986-C-T

52890712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74376134-C-T

http://identifiers.org/hco/4/GRCh38#52890926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74376308-C-A

52891061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74376440-G-C

52892546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74378203-G-A

http://identifiers.org/hco/4/GRCh38#52892687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74378308-C-A

52892824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74378426-C-T

52893466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74378830-C-G

52893466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74378830-C-T

52893654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74378960-C-G

52893767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74379067-T-C

52893792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74379092-T-C

52893855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74379144-C-T

52894109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74379332-T-A

52894407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74379619-A-G

52894411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74379623-T-C

52894424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74379636-G-C

52894549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74379758-T-C

52895123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74380207-T-A

52895154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74380242-G-C

52895155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74380243-C-T

52903505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74382608-T-C

http://identifiers.org/hco/4/GRCh38#52903513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74382616-A-C

52903558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74382654-G-A

52903644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74382728-C-T

52904241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74383584-T-C

52904254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74383597-T-A

52904289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74383630-C-T

52904385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74383720-C-T

52904475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74383810-C-G

52904475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74383810-C-T

52904567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74383890-G-A

52904612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74383940-C-T

52904679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74384004-G-A

52904747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74384063-C-T

52904820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74384135-T-G

52905110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74384373-G-T

52905111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74384374-T-C

52906397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74384941-C-T

52906508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74385056-C-T

52906603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74385167-G-A

52906603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74385167-G-C

http://identifiers.org/hco/4/GRCh38#52906848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74385414-C-A

52906870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74385436-C-G

52907365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74385851-G-T

52907765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74386287-A-G

52907846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74386562-T-C

52908121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74386826-G-C

52908222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74386921-G-C

52908486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74387189-C-T

52908504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74387206-A-G

52908528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74387230-C-T

52908700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74387386-T-A

52909022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74387646-T-A

52909485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74388172-G-A

52909748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74388398-G-T

52909959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74388573-G-A

52911386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74389818-C-T

52911569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74389964-G-A

52911733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74390104-C-T

52911862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74390209-G-A

52911881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74390226-G-A

52911882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74390227-G-A

52912615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74390579-C-T

52912637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74390601-C-G

52912637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74390601-C-T

52912655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74390607-T-A

52913787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74391002-G-T

52913983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74391202-T-C

52914353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74391550-G-T

52914537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74391685-G-A

52914552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74391700-G-A

52914552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74391700-G-C

52914579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74391720-C-T

52914673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74391791-C-G

52914733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74391859-T-G

52914735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74391861-A-G

http://identifiers.org/hco/4/GRCh38#52914960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74392143-C-A

52915265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74392344-G-C

52915426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74392476-A-G

52915807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74392823-G-A

52915807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74392823-G-C

52915853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74392883-T-C

52915876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74392903-G-C

52915921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74392948-C-T

52916153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74393176-C-T

52916167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74393189-C-T

52917340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74393786-C-T

52917709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74393998-A-T

52917908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74394146-G-A

52917923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74394158-T-C

52917941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74394170-C-T

52917945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74394174-T-C

52918021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74394255-A-G

52918101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74394328-A-G

52918273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74394753-T-C

52918312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74394792-T-C

52918395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74394854-C-T

52918397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74394856-A-T

52918512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74394972-A-G

52918565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74395046-A-G

http://identifiers.org/hco/4/GRCh38#52918803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74395270-C-A

52918803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74395270-C-T

http://identifiers.org/hco/4/GRCh38#52919029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74395492-C-A

52919057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74395519-G-T

52919203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74395665-C-T

52919867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74396260-A-G

http://identifiers.org/hco/4/GRCh38#52919915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74396321-A-C

52919930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74396335-C-T

52920093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74396493-T-A

52920336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74396729-A-G

http://identifiers.org/hco/4/GRCh38#52920569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74396946-C-A

52920569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74396946-C-T

http://identifiers.org/hco/4/GRCh38#52920575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74396952-A-C

52920614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74396991-T-C

52920648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74397024-G-A

52920648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74397024-G-T

52920664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74397042-T-C

http://identifiers.org/hco/4/GRCh38#52920667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74397045-A-C

52920684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74397061-T-C

52920839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: synonymous variant
orthologous variants: 74397214-G-A

http://identifiers.org/hco/4/GRCh38#52920909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74397284-C-A

52920973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74397342-T-C

52920973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74397342-T-G

52921019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74397360-G-A

52921019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74397360-G-T

52921046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74397387-C-T

52921109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74397449-C-T

52921143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74397483-C-T

52921157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74397498-C-T

52921159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74397500-G-A

52922676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74398017-T-C

52922705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74398046-A-G

52922972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74398258-C-G

52922972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74398258-C-T

52923033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74398319-G-A

http://identifiers.org/hco/4/GRCh38#52923676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74399382-A-C

52923676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74399382-A-G

52924044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74399802-T-C

http://identifiers.org/hco/4/GRCh38#52924288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74400098-A-C

52924288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74400098-A-G

52924288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74400098-A-T

52924312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74400120-G-A

52924325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74400133-G-A

52924502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74400247-T-C

52924743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74400457-G-C

52924749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74400463-T-C

52925055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74400627-C-T

52925513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74400966-G-A

52925526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74400979-T-C

52925661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74401114-C-T

http://identifiers.org/hco/4/GRCh38#52925716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74401149-C-A

52925820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74401251-C-G

52925958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74401386-A-T

52925969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74401394-C-G

52926012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74401436-C-T

52926078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74401492-A-G

52926088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74401502-C-T

52926621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74401980-C-T

52926726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74402077-C-T

52927505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74402852-C-T

52928630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74403605-G-A

52928630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74403605-G-C

52928639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74403614-C-T

52928777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74403713-G-A

http://identifiers.org/hco/4/GRCh38#52929036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74403965-A-C

52929283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74404231-A-G

http://identifiers.org/hco/4/GRCh38#52929306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74404284-C-A

52929306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74404284-C-T

52929387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74404379-C-G

52931145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74405605-G-A

52931145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74405605-G-C

52931145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74405605-G-T

http://identifiers.org/hco/4/GRCh38#52931278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74405739-C-A

52931278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74405739-C-G

52931494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74405929-G-C

52931500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74405935-T-C

52931757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74406167-C-G

52931794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74406205-T-C

52931804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74406215-T-C

52931829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74406243-A-G

52931888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74406304-C-T

http://identifiers.org/hco/4/GRCh38#52931979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74406381-A-C

52931979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74406381-A-G

52932013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74406413-A-G

52932046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 74406443-G-A

52932053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 74406450-T-C

52932524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74406944-G-A

52932753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74407174-A-G

52933194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74407600-A-G

52933200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74407606-C-T

52933224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74407614-C-T

52933225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74407615-G-A

52933225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74407615-G-T

52933530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74407902-G-T

52933542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74407910-G-C

http://identifiers.org/hco/4/GRCh38#52933622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74407973-C-A

52933622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74407973-C-G

52933622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74407973-C-T

52933658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74408011-A-T

52934128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74408092-A-G

52934190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74408152-C-T

http://identifiers.org/hco/4/GRCh38#52934368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74408306-C-A

52934547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74408547-G-A

52934712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74408693-A-G

52934808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74408774-T-C

52934818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74408781-C-T

52934832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74408796-T-G

52935187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74409922-G-C

http://identifiers.org/hco/4/GRCh38#52935281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74410032-C-A

52936127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74410207-G-A

52936131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74410211-C-G

52936131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74410211-C-T

52936134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74410214-G-T

52936211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74410283-G-A

52936227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74410295-C-T

52936299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74410365-T-G

52936354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74410410-A-G

52936355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74410411-A-G

52937049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74410960-G-A

52937049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74410960-G-C

52937072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74410981-G-A

52937072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74410981-G-T

52937410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74411273-C-G

52937572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74411429-T-C

52937630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74411484-T-C

52937821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74411636-C-T

52937844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74411659-G-C

52938223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74411955-T-C

52938641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74412337-T-C

52938747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74412414-T-C

http://identifiers.org/hco/4/GRCh38#52938748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74412415-C-A

52939143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74412956-A-G

52939420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74413222-G-T

52939433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74413235-G-A

52939534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74413348-A-G

52939635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74413433-A-T

52939686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74413483-A-G

52940087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74413855-T-C

http://identifiers.org/hco/4/GRCh38#52940302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74414122-A-C

52940359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74414255-T-C

52940387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74414299-G-A

52940387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74414299-G-T

http://identifiers.org/hco/4/GRCh38#52940896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74414777-C-A

52940896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74414777-C-T

52940987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74414839-A-G

52940994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74414846-C-G

52941103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74414963-C-T

52941134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74414991-A-T

52943906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74417669-G-T

52944099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74417851-C-T

52944200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74417954-G-T

52944268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74418009-A-G

52944330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74418096-A-G

52944400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74418207-T-G

http://identifiers.org/hco/4/GRCh38#52944468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74418270-A-C

52945750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74418503-T-C

52945804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74418570-A-G

52946163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74418926-C-G

52946163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74418926-C-T

52946966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74419645-A-G

52947254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74419895-G-A

52947308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74419948-G-A

52947495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74420204-T-C

52947781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74420483-G-C

http://identifiers.org/hco/4/GRCh38#52947788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74420500-C-A

http://identifiers.org/hco/4/GRCh38#52947991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74420663-C-A

52947991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74420663-C-G

52948017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74420689-G-T

52948072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74420737-A-G

52948265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74420912-A-G

52948321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74420963-G-A

52948321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74420963-G-T

52948522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421129-T-C

http://identifiers.org/hco/4/GRCh38#52948559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74421158-C-A

52948559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 74421158-C-T

52948572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421171-C-T

52948579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421178-T-C

52948580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421179-A-T

http://identifiers.org/hco/4/GRCh38#52948650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74421249-C-A

52948666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421265-T-C

http://identifiers.org/hco/4/GRCh38#52948677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74421276-C-A

52948677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421276-C-T

52948693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421292-C-T

52948695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421293-T-A

52948722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421316-C-T

52948763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421365-G-A

52948763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421365-G-T

http://identifiers.org/hco/4/GRCh38#52948795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74421397-C-A

52948795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421397-C-T

http://identifiers.org/hco/4/GRCh38#52949008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74421601-C-A

52949008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421601-C-G

52949009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421602-A-G

52949068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421636-T-A

52949068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421636-T-C

http://identifiers.org/hco/4/GRCh38#52949131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74421689-C-A

52949131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421689-C-G

52949319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421759-G-A

52949344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421784-G-T

52949602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74421992-T-C

52954603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74423847-G-A

52954665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74423901-A-G

52954750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74423977-G-C

52954910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74424110-C-T

52954937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74424132-C-G

http://identifiers.org/hco/4/GRCh38#52955922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74424978-C-A

52956135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425191-G-A

http://identifiers.org/hco/4/GRCh38#52956156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74425203-C-A

52956156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425203-C-G

52956172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425213-G-T

52956188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425233-T-A

52956188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425233-T-C

52956189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425234-C-T

http://identifiers.org/hco/4/GRCh38#52956190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74425235-C-A

52956190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425235-C-T

52956334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425366-G-A

52956347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425379-A-T

52956463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425466-T-C

52956564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425513-T-C

52956580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425528-T-C

52956829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425750-C-T

52956882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425783-G-A

52956882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425783-G-T

http://identifiers.org/hco/4/GRCh38#52957038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74425924-C-A

52957039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425925-T-A

52957039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74425925-T-C

http://identifiers.org/hco/4/GRCh38#52957210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74426071-C-A

52957289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74426150-A-G

52957360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74426221-T-C

52957393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74426268-G-A

52957442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74426322-C-T

52957614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74426482-G-A

52957614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74426482-G-T

52957650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74426518-C-T

52957660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74426528-A-G

http://identifiers.org/hco/4/GRCh38#52957885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74426729-C-A

52957911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74426745-C-T

52957940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74426774-G-A

52958322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74427134-G-A

52958380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74427193-T-A

http://identifiers.org/hco/4/GRCh38#52958903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74427671-C-A

52959098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74427853-A-T

52959189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74427913-G-C

52959409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74428090-G-A

52959456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74428134-A-G

52959461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74428139-C-G

52959571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74428244-A-G

52959577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74428249-C-T

52959750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74428414-A-G

52959903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74428551-C-T

52960742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74429022-C-T

http://identifiers.org/hco/4/GRCh38#52960746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74429031-A-C

52960975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74429294-G-A

52961414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74429667-G-A

52961418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74429671-G-A

52961533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74429788-G-A

52961693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74429921-T-C

52961782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74430006-T-G

52961792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74430016-C-T

52961882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74430112-G-A

52962222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74430388-G-T

52962358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74430512-C-T

52962368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74430522-A-G

52962674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74430754-G-A

52962674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74430754-G-C

52962674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74430754-G-T

52962755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74430816-G-A

52962829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74430872-G-A

52963017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74431052-G-C

52963017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74431052-G-T

52963022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74431057-T-C

52963146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74431311-T-C

52963334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74432045-G-A

52963612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74432301-T-G

52963891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74432789-T-C

52964062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74432962-T-C

http://identifiers.org/hco/4/GRCh38#52964117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74433017-C-A

52964152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74433052-T-C

52964255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74433154-A-T

52964368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74433248-C-T

52964449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74433335-G-T

52964484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74433368-C-T

52964568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74433451-G-A

52964586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74433469-G-A

52964859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74433697-A-G

52965124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74433957-G-C

52965240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74434086-C-T

52965721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74434536-C-T

52966030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74434855-A-G

52966889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74436525-A-G

52966918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74436559-G-A

52967224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74436830-T-C

http://identifiers.org/hco/4/GRCh38#52967259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74436866-C-A

52967303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74436898-T-A

52967500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74437092-C-G

52967500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74437092-C-T

52967527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74437120-T-C

52967583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74437175-T-C

52967661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74437241-A-G

52967679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74437259-T-C

52967902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74437445-C-T

52967959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74437499-T-G

52968038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74437543-T-C

52968315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74437734-G-A

52968462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74437871-C-T

52968645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74438030-A-G

52968701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74438085-G-T

52968762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74438136-G-A

http://identifiers.org/hco/4/GRCh38#52978171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74440038-A-C

52978281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74440140-G-A

52978564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74440580-A-G

52978628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74440644-T-C

52978661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74440674-A-G

52979146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74440922-A-G

52979339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74441096-T-G

52979375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74441133-C-T

52979412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74441176-T-C

52979739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74441452-C-T

52979763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74441475-C-T

52979835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74441537-G-T

http://identifiers.org/hco/4/GRCh38#52979843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74441545-C-A

52979843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74441545-C-T

52979970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74441652-C-G

http://identifiers.org/hco/4/GRCh38#52979981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74441663-C-A

52980016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74441698-T-C

52980054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74441732-T-C

http://identifiers.org/hco/4/GRCh38#52980075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74441751-C-A

52980214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74441851-C-T

52980390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74441953-G-A

http://identifiers.org/hco/4/GRCh38#52980482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74442020-C-A

52980845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74442263-A-T

52980912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74442326-C-T

52981036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74442452-T-C

52981353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74442888-A-G

52981497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74443022-T-C

52981768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74443316-C-T

http://identifiers.org/hco/4/GRCh38#52981892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74443435-C-A

52982112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74443837-C-G

52982140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74443865-T-C

52982192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74443909-T-C

52982281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74444007-G-A

52982287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74444013-G-C

52982295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74444021-T-C

52982378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74444089-G-A

52982382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74444093-G-A

52982472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74444160-T-C

52982732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74444380-T-A

52982732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74444380-T-G

52982752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74444400-A-T

52982803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74444451-T-C

52982803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74444451-T-G

52983030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74444690-C-T

52983091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74444751-A-G

52983248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74444855-T-C

52983672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74445186-T-C

52983715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74445218-C-T

52984140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74445625-G-C

http://identifiers.org/hco/4/GRCh38#52984177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74445657-C-A

52984195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74445674-T-C

52984301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74445750-A-G

52984597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74446057-A-G

52984632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74446092-G-T

http://identifiers.org/hco/4/GRCh38#52984796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74446193-C-A

52985083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74446448-G-A

52985542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74446893-C-G

52985542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74446893-C-T

52985604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74446945-C-T

52985674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74447026-A-G

52985674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74447026-A-T

52985856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74447210-T-C

52985910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74447254-G-T

52986907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74447778-A-G

52987563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74448168-T-C

52987563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74448168-T-G

52987918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74448334-C-T

http://identifiers.org/hco/4/GRCh38#52988015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74448434-C-A

52988249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74448597-C-T

52988258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74448606-T-C

52988423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74448770-T-A

http://identifiers.org/hco/4/GRCh38#52988566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74448910-C-A

52988566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74448910-C-G

52988765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74449114-C-T

52988838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74449180-G-A

52989041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74449851-T-C

52989050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74449857-A-G

52989171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74449968-G-C

http://identifiers.org/hco/4/GRCh38#52989212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74450005-C-A

52989212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74450005-C-T

52989408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74450169-C-T

52989611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74450382-C-T

52989616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74450384-G-A

52989657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74450415-T-A

52989657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74450415-T-C

52990001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74450708-G-A

52990131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74450835-T-G

52990298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74450999-T-A

52990395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74451096-T-A

http://identifiers.org/hco/4/GRCh38#52990453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74451154-C-A

52990453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74451154-C-T

52990918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74452252-A-G

52990918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74452252-A-T

52991074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74452386-C-G

52991158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74452457-T-C

52991495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74452788-T-A

52991495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74452788-T-C

http://identifiers.org/hco/4/GRCh38#52991566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74452864-A-C

52991566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74452864-A-G

52991874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74453141-T-G

52991949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74453215-A-T

http://identifiers.org/hco/4/GRCh38#52993624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74453401-A-C

52994778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74454422-T-A

52994791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74454435-A-G

52994881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74454503-A-G

52994898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74454520-T-C

52994905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74454525-C-T

52994967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74454582-G-A

52996299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74456195-G-A

52996363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74456225-G-A

52996481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74456332-T-C

52996577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74456416-G-C

52996678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74456508-A-G

52996949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74456701-G-T

52997125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74456850-A-G

52997329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74457040-G-A

52998912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74457578-G-C

http://identifiers.org/hco/4/GRCh38#53000198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74459152-C-A

53000198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74459152-C-T

53000309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74459256-T-G

53000361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74459309-G-C

53000640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74459594-G-A

53000641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74459595-G-T

53004309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74461154-C-T

53004511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74461321-A-G

53004561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74461367-T-C

53005300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74461716-A-G

53005701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74462060-A-G

53005800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74462172-A-G

53005800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74462172-A-T

53006492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74462793-A-G

53006539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74462839-T-C

53006633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74462906-C-G

53006633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74462906-C-T

http://identifiers.org/hco/4/GRCh38#53009327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74464124-C-A

53009722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74464497-C-G

53009722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74464497-C-T

53009737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74464643-T-G

53009740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74464646-G-C

53009921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74464978-C-G

53010353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74465417-G-A

53010377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74465444-G-C

53010391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74465473-A-G

53010416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74465498-A-G

53010484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74465568-C-G

53010518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74465602-T-C

53011191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74466238-G-A

53011654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74466681-T-A

53011655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74466682-C-T

53011699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74466726-C-T

53011737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74466758-G-A

53011975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74466980-G-T

53011977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74466982-A-G

53012328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74467490-T-G

53012353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74467512-C-G

53012353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74467512-C-T

53012354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74467513-T-G

53012371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74467575-C-G

53012430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74467631-T-G

53012464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74467667-A-T

53012489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74467693-A-G

53012635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74467826-C-T

53012809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74467990-C-T

53012853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74468011-A-T

53012873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74468031-G-T

53012925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74468083-C-G

53012961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74468119-A-T

53013023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74468179-G-A

53013052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74468206-G-A

http://identifiers.org/hco/4/GRCh38#53013058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74468222-A-C

53013160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74468370-G-A

53013394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74468583-G-A

53013889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74470432-C-T

53014114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74470659-A-G

53014149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74470695-G-A

53014233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74470771-G-A

53014234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74470772-T-A

53014329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74470843-G-T

53014454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74470962-A-G

53014702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74471196-C-T

53014932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74471418-A-T

53014951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74471437-T-C

http://identifiers.org/hco/4/GRCh38#53014978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74471466-C-A

53014978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74471466-C-T

53015122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74471615-T-G

53015526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74471990-C-T

53015582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74472040-C-T

53015619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74472080-C-T

53015811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 74472258-C-T

53015848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 74472281-T-C

53016064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 74472480-A-T

http://identifiers.org/hco/4/GRCh38#53016318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74472735-A-C

53016439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74472859-C-T

53016503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74472928-T-A

53016763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74473167-G-C

53017239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74473387-G-A

http://identifiers.org/hco/4/GRCh38#53017637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74473989-A-C

53017730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74474608-C-G

http://identifiers.org/hco/4/GRCh38#53017818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74474696-C-A

53017895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74474731-C-T

53017896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74474732-G-A

53017896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74474732-G-T

53018170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74474946-G-T

53018676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74475418-C-T

53018830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74475569-C-T

53018951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74475673-A-G

53019056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74475782-C-G

53019056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74475782-C-T

53019537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74476241-C-G

53019589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74476286-T-G

53019908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74476575-G-A

53019994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74476660-C-G

53019994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74476660-C-T

53020238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74476901-T-A

53020742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74478068-G-A

53020742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74478068-G-T

53021101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74480976-A-G

53021612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74481481-G-A

53021714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74481579-G-C

53021718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74481583-T-C

53021851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74481727-T-A

53021851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74481727-T-C

53021951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74481827-T-G

http://identifiers.org/hco/4/GRCh38#53021986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74481860-A-C

53022023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74481897-G-A

53022585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74483487-T-C

53022667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74483567-G-T

53023554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74484488-C-T

53023642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74484623-C-G

53023642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74484623-C-T

53023643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74484624-A-G

53024308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74486965-A-G

53024470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74487087-T-C

53024506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74487126-G-A

53024800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74487398-T-G

53024844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74487440-C-T

53024894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74487486-T-C

53024919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74487509-G-T

53024926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74487516-C-T

53025015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74487610-A-T

53025566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74488137-G-T

53025704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74488266-G-C

53026541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74488774-A-G

http://identifiers.org/hco/4/GRCh38#53026623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74488821-C-A

53027065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74489205-T-C

53027159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74489294-C-G

53027160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74489295-A-T

53027183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74489317-C-G

53027273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74489398-C-T

53027277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74489411-G-T

53027309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74489444-G-C

http://identifiers.org/hco/4/GRCh38#53027834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74489787-A-C

53027901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74489838-A-T

53027906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74489843-T-A

53027906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74489843-T-C

53027934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74489872-G-A

53027964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74489907-T-A

53027964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74489907-T-C

53027989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74489933-G-A

53028704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74490549-C-G

53028728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74490570-T-G

53028909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74490733-G-C

53028994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74490817-T-G

http://identifiers.org/hco/4/GRCh38#53029257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74491117-C-A

53029411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74491273-T-C

53029428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74491290-T-C

53029579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74491402-G-A

53029640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74491457-T-A

53030183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74491971-T-G

53030185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74491973-A-T

53036941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74492551-C-T

53037483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74493420-T-C

53037670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74494011-T-C

53037959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74494268-T-C

53038094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74494402-A-G

53038214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74494525-T-A

53038332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74494637-T-C

53038371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74494680-G-T

53041112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74495826-G-C

53041459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74496159-C-T

53041511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74496215-T-C

53041757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74496409-C-T

53042003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74496593-T-C

53042376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74496874-T-C

53042408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74496904-T-C

53042721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74497117-G-T

http://identifiers.org/hco/4/GRCh38#53042722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74497118-C-A

53042722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74497118-C-T

53042723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74497119-C-G

53042815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74497210-T-A

53043088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74497427-C-T

53043231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74497557-G-C

53043454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74497770-C-G

53043570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74497869-G-A

53043580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74497879-G-A

53043662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74497946-A-G

53043836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74498141-A-G

53044063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74498352-G-A

53044343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74498570-G-A

53044343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74498570-G-C

53048680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74502208-G-A

53048715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74502239-T-C

http://identifiers.org/hco/4/GRCh38#53049968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74501417-A-C

53049968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74501417-A-G

53050097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74501532-A-G

53050147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74501583-T-G

53050196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74501626-T-G

53050564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74502091-G-A

53050727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74502208-C-T

http://identifiers.org/hco/4/GRCh38#53054435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74502462-C-A

53054435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74502462-C-T

53054991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74502908-G-A

http://identifiers.org/hco/4/GRCh38#53055132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74503033-C-A

53055132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74503033-C-T

http://identifiers.org/hco/4/GRCh38#53055139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74503040-C-A

53055277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74503223-T-G

53055354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74503312-T-C

53055466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74503425-G-A

53055787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74503795-T-C

53055813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74503819-C-T

53055968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74503967-C-G

53056313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74504316-C-T

53056314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74504317-G-A

53056376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74504371-G-C

53056638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74504602-T-C

53056825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74504782-A-T

53058065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74505174-T-A

53058520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74505725-C-T

53059584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74506323-G-C

53059584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74506323-G-T

53059762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74506489-T-C

53060170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74507286-T-A

53060284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74507390-C-T

53060775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74508489-G-A

53060819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74508533-A-T

53060940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74508649-T-C

53060940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74508649-T-G

http://identifiers.org/hco/4/GRCh38#53061163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74508773-A-C

53061191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74508801-C-T

53061192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74508802-A-G

53061222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74508833-T-C

53061413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74509002-C-G

53061449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74509045-A-G

53061449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74509045-A-T

53061949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74509491-C-T

53062744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74510248-G-A

53062744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74510248-G-T

53062881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74510371-T-C

53064984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74511549-A-G

53065186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74511740-A-T

53065203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74511757-C-T

53065204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74511758-G-A

53065227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74511780-T-C

53065429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74511954-A-G

53065606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74512123-T-C

53065624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74512141-C-T

53065642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74512160-C-G

53065778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74512300-G-T

53066625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74513143-T-G

53066646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74513166-C-T

53067335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74513811-G-C

53067364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74513839-C-T

53068687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74514672-G-A

53068892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74514934-C-T

53069267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74515311-A-T

53069271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74515315-G-A

53069372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74515405-T-A

53069402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74515416-T-C

53069488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74515481-C-T

53069538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74515527-C-T

53069567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74515551-G-C

53069893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74515953-T-A

53069894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74515954-A-G

http://identifiers.org/hco/4/GRCh38#53069896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74515956-A-C

53070066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74516117-G-C

http://identifiers.org/hco/4/GRCh38#53070381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74516425-A-C

53070381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74516425-A-G

53070879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74516831-A-G

53073529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74521761-T-C

53073553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74521783-G-C

53073553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74521783-G-T

53073581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74521809-G-A

53076049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74521895-T-C

53076149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74521988-C-T

53076498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74522334-C-T

53076683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74522518-T-C

53076707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74522542-T-G

53076763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74522603-C-T

53076773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74522613-T-C

53076865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74522793-G-T

53076945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74522854-G-A

53076945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74522854-G-C

53077045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74522942-T-C

53077104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74523050-G-C

53077209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74523217-C-G

http://identifiers.org/hco/4/GRCh38#53077212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74523220-C-A

53077212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74523220-C-T

53077426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74523419-T-C

53078085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74524140-T-C

http://identifiers.org/hco/4/GRCh38#53078503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74524818-C-A

53078503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74524818-C-T

53078831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74525160-T-G

53078859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74525190-T-C

53079200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74525285-C-T

53079951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74526293-T-A

53080016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74526331-G-C

53080116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74526423-G-A

http://identifiers.org/hco/4/GRCh38#53080205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74526499-A-C

53080463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74526843-G-A

http://identifiers.org/hco/4/GRCh38#53080661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74527147-C-A

53081020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74527499-A-G

53081062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74527528-C-T

53081090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74527553-C-T

53081114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74527576-G-A

53081943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74528131-G-A

53081943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74528131-G-T

53082016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74528189-T-C

53082079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74528245-T-C

53082106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74528268-C-T

53082148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74528315-A-G

53082249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74528398-T-C

53082267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74528414-A-T

http://identifiers.org/hco/4/GRCh38#53082418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74528521-A-C

53082418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74528521-A-G

http://identifiers.org/hco/4/GRCh38#53082563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74528641-A-C

53082696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74528747-C-G

53083032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74529001-G-T

53083067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74529035-G-C

53083261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74529221-A-G

53087998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74532487-G-A

53088242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74532700-T-C

53088247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74532706-C-G

53088385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74532865-G-A

53088478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74532962-C-T

53088595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74533084-C-G

http://identifiers.org/hco/4/GRCh38#53088793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74533288-C-A

53088793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74533288-C-T

53088907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74533504-T-C

53088927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74533522-T-G

53089068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74533629-C-T

53089179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74533743-T-C

53089187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74533750-G-A

http://identifiers.org/hco/4/GRCh38#53089189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74533752-C-A

53089191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74533754-A-G

http://identifiers.org/hco/4/GRCh38#53089475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74534017-C-A

http://identifiers.org/hco/4/GRCh38#53089653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74534186-C-A

53089686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74534224-A-G

53090157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74535754-A-G

53090470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74536117-G-A

53090603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74536255-C-T

53091086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74536639-G-A

53091121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74536674-T-C

53091256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74536814-A-T

53091398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74536873-G-A

53091407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74536882-G-A

53091548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74537024-C-T

53091571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74537044-T-C

53092028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74537597-T-C

53092573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74538311-A-G

53092635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74538368-G-A

53092635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74538368-G-C

53099236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74538842-A-G

53099237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74538843-T-C

53099296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74538913-G-C

53099942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74539591-T-A

53099942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74539591-T-C

53100263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74539879-T-A

53100426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74540037-C-T

53100434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74540045-C-T

53100714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74540589-T-C

53100959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74540830-C-T

53101021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74540891-C-T

53102056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74541778-T-C

53102459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74542317-T-G

53102641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74542474-A-G

53118056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74543940-A-G

53118057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74543941-T-C

53118426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74545167-T-A

53118974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74545643-G-C

53119662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74545839-T-C

53119789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74545948-C-T

53119943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74546092-T-C

53120208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74546257-C-T

53120243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74546294-A-G

53120260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74546311-C-G

53120509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74546537-T-C

http://identifiers.org/hco/4/GRCh38#53121006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74546950-C-A

53121131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74547076-C-G

53121131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74547076-C-T

53121346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74547265-C-T

53121464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74547396-C-T

53127000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74547562-A-T

53127133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74547694-C-T

53127144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74547705-A-G

53127266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74547812-T-G

53127538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74548069-G-C

53127711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74548229-T-C

53127788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74548302-G-T

53127936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74548448-G-T

53127962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74548461-C-T

53127991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74548478-A-T

http://identifiers.org/hco/4/GRCh38#53128071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74548641-C-A

http://identifiers.org/hco/4/GRCh38#53128093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74548667-C-A

53128093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74548667-C-T

http://identifiers.org/hco/4/GRCh38#53128169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74548741-C-A

53128169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74548741-C-T

53128699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74549256-C-T

53128701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74549258-T-G

53129045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74549552-A-G

53129073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74549582-T-G

53129333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74549808-A-G

53129475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74549944-C-T

http://identifiers.org/hco/4/GRCh38#53129497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74549976-A-C

http://identifiers.org/hco/4/GRCh38#53129824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74550544-C-A

53131982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74551876-T-A

53131982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74551876-T-C

http://identifiers.org/hco/4/GRCh38#53132154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74552036-A-C

53132154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74552036-A-G

53132155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74552037-T-A

53132155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74552037-T-C

53132238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74552121-T-G

53132460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74552344-C-T

http://identifiers.org/hco/4/GRCh38#53132635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74552499-A-C

53132752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74552616-T-C

53132752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74552616-T-G

53136757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74554077-C-G

53136982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74554300-C-G

53136982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74554300-C-T

53137583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74554760-A-T

53137643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74554824-T-C

53138287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74555152-C-G

53138423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74555272-A-G

53138518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74555367-G-C

http://identifiers.org/hco/4/GRCh38#53140427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74555701-A-C

53140427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74555701-A-T

53140576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74555846-T-C

53140715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74555977-C-T

53140716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74555978-G-A

53140787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74556033-G-A

53142390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74556251-A-T

53142488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74556363-G-A

53142514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74556375-C-T

53142699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74556545-A-G

53142870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74556792-T-C

53143447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74557348-G-A

53143447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74557348-G-T

53143650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74557559-G-C

53143670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74557579-G-A

53144776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74558191-T-C

53145436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 74558418-C-G

53145436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 74558418-C-T

53145556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 74558538-A-G

53145565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 74558547-T-C

53145565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 74558547-T-G

53145595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74558579-A-G

53145595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74558579-A-T

53145619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74558600-G-A

53145660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74558641-G-T

53145723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74558697-G-T

53145777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74558751-C-T

53146137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74559274-C-T

53146319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74559709-T-C

53148102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74560290-A-G

53148456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74560608-C-G

53150609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74561946-G-A

53150649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562006-C-T

53150686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562043-C-T

53150844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562201-T-C

53150891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562246-G-C

53151014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562334-A-G

53151034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562354-C-G

http://identifiers.org/hco/4/GRCh38#53151124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74562447-A-C

53151179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562500-C-T

53151293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562614-G-T

53151388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562708-G-A

53151470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562787-T-G

53151513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562806-C-G

53151513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562806-C-T

53151526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562819-G-A

53151608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562879-G-A

53151673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562930-A-G

53151673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74562930-A-T

http://identifiers.org/hco/4/GRCh38#53155044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74566023-A-C

53155355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74566326-C-T

53156768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74566856-T-C

53157216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74567443-C-T

http://identifiers.org/hco/4/GRCh38#53157607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74567835-C-A

53157607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74567835-C-T

53157618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74567848-T-C

53157936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74568322-T-A

53157936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74568322-T-C

53157956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74568342-G-A

53160237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74571402-T-G

53160321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74571488-G-A

53160321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74571488-G-T

53160339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74571506-G-A

53160535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74571685-G-C

53160623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74571735-C-G

53160624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74571736-T-C

53160785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74571826-A-G

53160795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74571834-G-A

http://identifiers.org/hco/4/GRCh38#53161318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74572498-A-C

53161549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74572723-G-A

53161549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74572723-G-C

53161559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74572733-A-T

53161675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74572852-C-T

53162920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74573772-C-T

53163110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74573925-G-A

53163242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74574014-T-C

http://identifiers.org/hco/4/GRCh38#53163285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74574054-C-A

53164219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74574635-G-A

http://identifiers.org/hco/4/GRCh38#53164345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74574770-A-C

53164433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74574856-T-A

53164448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74574871-T-C

53164461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74574884-G-A

53164475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74574898-G-A

http://identifiers.org/hco/4/GRCh38#53174346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74575654-C-A

53174601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74576231-C-T

53174644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74576289-G-A

53174738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74576385-G-C

53174738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74576385-G-T

http://identifiers.org/hco/4/GRCh38#53175064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74576683-C-A

53175064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74576683-C-G

53175142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74576764-C-T

53175408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74576992-A-G

53175442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74577028-G-C

53175554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74577119-C-T

53175660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74577219-T-G

53175755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74577287-G-T

53176095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74577604-T-C

53176302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74578039-C-G

53176302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74578039-C-T

53176353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74578089-T-C

53176363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74578100-T-A

53176372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74578109-C-T

53176466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74578212-A-G

53176557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74578298-T-A

53176585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74578327-G-A

53176585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74578327-G-T

53177184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74578678-G-T

53177319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74578847-C-G

53177414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74578938-G-A

53183766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74579069-G-T

53184115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74579687-G-A

53184392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74579960-G-T

53184602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74580146-C-T

53185267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74580254-T-C

53185315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74580303-G-T

53186051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74581190-A-G

53186116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74581271-G-A

http://identifiers.org/hco/4/GRCh38#53186141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74581331-C-A

53186141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74581331-C-T

53186322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74581508-T-C

53186364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74581546-C-T

http://identifiers.org/hco/4/GRCh38#53186507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74581693-A-C

53186778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74581939-G-A

53186894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74582045-T-C

53187058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74582183-T-C

http://identifiers.org/hco/4/GRCh38#53187264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74582434-C-A

53187264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74582434-C-G

53187553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74582648-A-G

53187610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74582689-G-A

53187610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74582689-G-T

53187711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74582789-G-T

http://identifiers.org/hco/4/GRCh38#53188511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74583464-C-A

53188646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74583574-G-A

53188891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74583758-C-T

53188910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74583772-A-T

53189042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74583859-A-G

53189222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74584115-A-G

53189391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74584325-T-C

53189468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74584400-G-T

53189497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74584505-C-G

53189517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74584524-G-T

53189525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74584532-C-T

53189528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74584535-G-A

53189563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74584584-T-C

http://identifiers.org/hco/4/GRCh38#53189640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74584735-C-A

53189641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74584736-C-T

53189862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74584926-T-C

53189862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74584926-T-G

53189912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74584974-T-C

53192758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74589707-G-C

53193138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74590178-G-A

53193318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74590362-G-A

53193437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74590471-C-T

53193650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74590661-T-C

53193759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74590778-C-G

53193885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74590906-C-G

http://identifiers.org/hco/4/GRCh38#53194101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74591087-C-A

53194109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74591095-T-C

53194431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74591402-T-C

53194459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74591429-T-C

53194576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74591544-G-C

53194589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74591590-G-A

53194800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74591804-C-G

53194948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74591908-A-G

53194958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74591918-T-C

53195040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74592295-A-T

53195047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74592302-G-A

53195047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74592302-G-T

53195386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74592726-T-C

53195491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74592804-A-G

53195660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74592980-A-G

53195681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74593001-A-G

53195739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74593052-C-G

53195817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74593129-G-C

53195874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74593186-T-C

53196290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74593604-T-C

http://identifiers.org/hco/4/GRCh38#53196536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74593850-C-A

53196536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74593850-C-T

http://identifiers.org/hco/4/GRCh38#53196737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74594051-C-A

53196920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74594228-T-C

53197204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74594482-G-A

53197204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74594482-G-T

53197253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74594520-T-C

http://identifiers.org/hco/4/GRCh38#53197430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74594696-A-C

53198001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74595237-T-G

53198066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74595304-C-T

53198099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74595338-T-C

53198225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74595663-G-A

53198530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74595947-C-T

53198631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74596026-G-C

http://identifiers.org/hco/4/GRCh38#53198725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74596096-C-A

53199300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74596632-T-C

53200049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74597910-C-T

53200145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74597981-G-A

53200259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74598073-C-G

53200442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74598263-T-A

53200442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74598263-T-C

53200462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74598288-T-A

53200468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74598294-T-A

http://identifiers.org/hco/4/GRCh38#53200509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74598335-A-C

53200512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74598338-G-C

53200569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74598392-T-C

53200643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74598467-A-G

53200643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74598467-A-T

53200860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74598703-T-C

53200919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74598765-A-G

53203347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74598853-G-T

53203398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74598905-C-T

53203537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74599043-G-A

53203537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74599043-G-C

53204015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74599231-T-A

53204212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74599409-C-T

http://identifiers.org/hco/4/GRCh38#53204272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74599467-A-C

53207468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74604792-G-T

http://identifiers.org/hco/4/GRCh38#53209469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74605670-A-C

53209583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74605776-C-T

53209823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74606185-T-C

53209865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74606223-T-G

53209884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74606242-A-G

53209885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74606243-G-A

53209899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74606258-T-A

53209909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74606273-T-C

53210089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74606435-T-C

53210280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74606605-G-C

53210363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74606677-T-A

53210364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74606678-C-T

53210541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74606859-C-T

53211985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74607396-G-A

53212086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74607487-A-T

53212087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74607488-C-T

53212213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74607587-C-G

53212234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74607608-A-G

53212346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74607701-C-G

53212366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74607721-A-G

53212388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74607743-C-T

53212389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74607744-A-G

53212512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74607807-A-G

53212891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74608100-T-G

53212912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74608121-T-G

53213006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74608604-G-A

53213006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74608604-G-T

53213089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74608687-A-G

53213197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74608797-C-T

53213236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74608833-G-A

53213236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74608833-G-T

53213248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74608845-T-C

53213316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74608908-G-A

53213451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74609050-G-C

53213458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74609057-T-C

53213495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74609120-T-A

53213495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74609120-T-C

53221519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74611135-C-T

53221535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74611153-T-G

http://identifiers.org/hco/4/GRCh38#53221541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74611159-C-A

53221541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74611159-C-T

53221692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74611290-G-T

53221693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74611291-T-C

53222077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74611600-C-T

http://identifiers.org/hco/4/GRCh38#53222088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74611607-A-C

53222088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74611607-A-G

53222107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74611626-A-G

53222131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74611650-G-A

53222142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74611661-T-A

53222147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74611666-C-T

53222201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74611709-A-T

53222255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74611753-A-G

53222328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74611831-A-G

http://identifiers.org/hco/4/GRCh38#53222380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74611863-A-C

53222672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74612183-G-A

53222692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74612203-G-C

53223085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74612580-G-A

53223213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74612715-C-G

53233425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74614104-C-T

53233670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74614337-T-C

53234044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74615223-C-T

53234234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74615388-A-G

53234325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74615482-G-C

http://identifiers.org/hco/4/GRCh38#53234414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74615575-C-A

53234519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74615650-G-C

53264668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74616859-G-T

53264843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74617027-G-C

53264865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74617050-A-G

53264977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74617168-G-A

53264977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74617168-G-T

53266737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74618387-A-G

53266832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74618473-A-T

http://identifiers.org/hco/4/GRCh38#53267086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74618644-C-A

53267107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74618666-T-C

53269499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74619436-A-G

53272966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74622107-T-A

53273021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74622163-T-A

53273021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74622163-T-C

53273298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74622400-G-T

53273403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74622506-C-T

53273452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74622555-T-C

53273479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74622582-T-C

53273563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74622665-G-T

http://identifiers.org/hco/4/GRCh38#53273588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74622690-C-A

53273691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74622781-G-A

53273691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74622781-G-T

53273815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74623210-T-C

53273970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 74623365-A-G

53274138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74623530-G-T

53274411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74623755-A-G

53274426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74623765-G-C

53274864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74624234-T-C

53275119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74624455-G-A

53276728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74626113-A-T

53277178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74626506-A-G

53277190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74626518-A-G

53278565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74627300-G-T

53278674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74627398-T-C

53281142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74628702-T-C

53281772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74629460-T-A

53284420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74630014-G-T

53284610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74630213-G-A

53284738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74630345-T-C

53284781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74630397-A-G

53285068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74630677-A-G

53285286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74630871-T-C

53285436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74631013-A-G

53285583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74631154-A-G

53285885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74631633-C-T

53286074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74631823-C-T

53286133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74631871-C-T

53306089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74637009-C-T

http://identifiers.org/hco/4/GRCh38#53306118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74637038-C-A

53306231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74637167-G-T

53306417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74637342-C-T

53306617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74637499-G-T

http://identifiers.org/hco/4/GRCh38#53306618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74637500-C-A

53306618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74637500-C-T

53306654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74637541-A-T

53306655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74637542-C-T

53306748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74637613-G-A

53306762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74637633-G-A

53307127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74638047-A-G

53307231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74638153-T-C

53307287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74638207-C-G

53307287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74638207-C-T

53307319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74638239-A-G

http://identifiers.org/hco/4/GRCh38#53307341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74638266-A-C

http://identifiers.org/hco/4/GRCh38#53307481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74638387-C-A

53307481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74638387-C-G

53308114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron_variant, undefined
orthologous variants: 74639050-T-C

http://identifiers.org/hco/4/GRCh38#53308388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74639310-C-A

53308447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74639377-C-G

53308643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74639559-T-C

53308644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74639560-T-C

53309991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74639691-T-C

53310088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74639766-G-C

53310158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74639836-T-C

53310243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74639904-T-C

53310323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74639959-G-T

53310351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74639987-T-C

53310374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74640009-T-C

http://identifiers.org/hco/4/GRCh38#53310620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74640215-A-C

53310875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74640438-A-G

53311102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74640705-T-C

53311220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74640805-T-A

53313618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74642793-T-A

53313630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74642805-G-A

http://identifiers.org/hco/4/GRCh38#53313787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74642959-C-A

53313787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74642959-C-G

53315234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74644631-G-A

53315647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74644843-C-T

53315862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74645055-G-T

53316080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74645287-G-A

53316177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74645359-T-A

53316208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74645394-T-C

53318537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74649801-A-G

http://identifiers.org/hco/4/GRCh38#53319332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74650766-C-A

53320720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74652189-G-A

53320751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74652220-A-T

53321209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74653245-G-A

53321383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74653420-T-C

53321488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74653539-G-A

53321488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74653539-G-C

53321491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74653542-G-T

53321561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74653611-T-G

53321645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30676
most severe consequence: intron variant
orthologous variants: 74653703-C-T