http://identifiers.org/hco/3/GRCh38#193274807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29051137-C-A

193274811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 29051141-T-G

193274855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 29051184-G-A

193274855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 29051184-G-T

http://identifiers.org/hco/3/GRCh38#193274873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29051196-A-C

193274874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 29051197-A-G

193274890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29051209-T-C

193274890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29051209-T-G

193274927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29051247-T-C

193275030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29051343-C-T

193275113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29051426-C-T

http://identifiers.org/hco/3/GRCh38#193275352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29051674-C-A

193275352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29051674-C-T

193275356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29051678-C-T

193275366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29051680-G-A

193275366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29051680-G-T

http://identifiers.org/hco/3/GRCh38#193275395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29051708-C-A

http://identifiers.org/hco/3/GRCh38#193275433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29051746-C-A

193275433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29051746-C-T

193275476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29051766-G-A

193275490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29051780-C-T

193275605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29051962-C-T

193275606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29051963-G-A

193275685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29052057-G-T

193275905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29052477-G-A

193275951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29052521-A-G

http://identifiers.org/hco/3/GRCh38#193276036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29052586-A-C

193276077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29052636-G-A

193276136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29052716-A-G

193276410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29052973-T-C

193276444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053004-G-C

193276494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053053-A-G

193276518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053076-C-G

193276518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053076-C-T

193276519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053077-A-G

193276653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053211-G-T

193276661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053219-A-G

193276673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053231-C-G

193276674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053232-T-C

http://identifiers.org/hco/3/GRCh38#193276688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29053246-C-A

193276688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053246-C-T

193276702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053260-A-G

193276702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053260-A-T

http://identifiers.org/hco/3/GRCh38#193276704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29053262-C-A

193276783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 29053344-G-A

193276783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 29053344-G-T

193276828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 29053389-C-T

193276852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053419-T-C

http://identifiers.org/hco/3/GRCh38#193276871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29053438-C-A

193276871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053438-C-T

http://identifiers.org/hco/3/GRCh38#193276961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29053560-A-C

193276961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 29053560-A-T

193276969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053568-T-A

193276969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053568-T-C

193276969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053568-T-G

http://identifiers.org/hco/3/GRCh38#193276977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29053576-A-C

193276977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053576-A-G

193276977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 29053576-A-T

193276978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053577-A-G

193276978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053577-A-T

193277125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 29053740-A-G

193277504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29054130-G-T

193277569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29054199-C-G

http://identifiers.org/hco/3/GRCh38#193277577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29054207-C-A

193277577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29054207-C-T

193277778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29054376-A-G

http://identifiers.org/hco/3/GRCh38#193277779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29054377-C-A

http://identifiers.org/hco/3/GRCh38#193277794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29054394-C-A

193278230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29054717-A-G

193278522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29054996-G-A

193279249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29055868-T-C

193279249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29055868-T-G

193279257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29055874-C-T

193279266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29055883-G-A

193279319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29055937-G-T

193279324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29055942-T-C

193279324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29055942-T-G

193279336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29055956-A-G

193279376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29055995-C-T

http://identifiers.org/hco/3/GRCh38#193279423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29056042-C-A

193279423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29056042-C-G

193279533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29056147-T-C

193279556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29056171-A-G

193279556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29056171-A-T

193279691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29056301-C-T

http://identifiers.org/hco/3/GRCh38#193280622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29056895-C-A

193280622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29056895-C-T

193280645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29056918-T-C

http://identifiers.org/hco/3/GRCh38#193281074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29057217-A-C

193281074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29057217-A-G

http://identifiers.org/hco/3/GRCh38#193281127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29057266-C-A

http://identifiers.org/hco/3/GRCh38#193281260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29057398-C-A

193281306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29057444-T-C

193281334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29057458-T-G

http://identifiers.org/hco/3/GRCh38#193281585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29057688-A-C

193281609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29057724-G-A

193281666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29057779-G-C

193282207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29058824-A-G

193282848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29062531-C-T

193282912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29062584-G-T

193283143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29062810-T-C

193283539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29063209-C-G

193283648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29063326-G-A

193283655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29063333-T-A

193284794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29066780-T-C

193284794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29066780-T-G

193284809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29066795-A-T

193284812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29066798-G-T

http://identifiers.org/hco/3/GRCh38#193284838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29066810-C-A

193284838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29066810-C-T

193284840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29066812-G-T

193285002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29066974-T-C

193285077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29067049-A-G

193285103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29067075-C-T

193285202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29067181-T-C

193285236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29067215-A-G

http://identifiers.org/hco/3/GRCh38#193285246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29067225-C-A

193285734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29068125-C-T

193285752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29068143-T-C

193285772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29068163-C-T

193285836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29068208-G-A

193285907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29068248-G-A

193286044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29068355-A-T

193286160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29068471-T-A

193286165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29068476-A-T

193288791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29069199-A-G

193288831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29069238-T-C

193288908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29069303-C-T

193289025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29069426-T-C

http://identifiers.org/hco/3/GRCh38#193289590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29069701-A-C

193289682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29069794-C-T

193289845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29069963-A-T

193289849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29069967-T-A

http://identifiers.org/hco/3/GRCh38#193290099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29070216-C-A

193290152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070262-G-T

193290252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070362-C-T

193290328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070437-A-G

193290552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070624-T-C

193290681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070752-G-C

193290861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070913-G-T

193290872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070924-G-A

193291133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29071179-T-G

193291267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29071320-G-A

193291361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29071393-C-G

193291537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29073137-G-A

193291537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29073137-G-T

193291770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29073344-G-A

193291914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29073479-A-G

http://identifiers.org/hco/3/GRCh38#193292240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29073794-A-C

193292576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29074507-C-G

193292687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29074596-T-A

193292687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29074596-T-C

193292751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29074654-C-G

193293001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29074876-A-G

193293066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29074941-A-G

193293329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29075187-G-T

193293347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29075205-A-G

193293554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29075413-A-G

193293554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29075413-A-T

http://identifiers.org/hco/3/GRCh38#193293892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29075695-C-A

193293892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29075695-C-T

193293909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29075712-G-T

193293959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29075758-G-A

193294237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29076023-A-T

193294419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29076193-C-T

193298240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29078572-C-T

193298433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29078767-A-G

193298464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29078797-G-A

193298464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29078797-G-T

http://identifiers.org/hco/3/GRCh38#193299267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29079796-C-A

193299285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29079812-G-A

193299285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29079812-G-T

193299296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29079827-G-T

193299542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29080052-T-A

193299682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29080406-G-A

193299727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29080451-G-A

193299784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29080511-T-C

193299849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29080562-T-C

193299857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29080570-A-G

193299939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29080645-G-T

193300009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29080708-G-A

193300011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29080710-C-T

193300109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29081031-G-A

193300254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29081289-C-T

193300389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29081431-C-T

193300694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29081696-G-A

193300772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29081774-A-G

193301250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29082237-G-A

http://identifiers.org/hco/3/GRCh38#193301453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29083141-A-C

193301453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29083141-A-T

193301751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29083418-T-A

193301761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29083428-C-T

193301787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29083452-A-T

193301861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29083525-G-C

193302016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29083666-T-C

193302045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29083693-T-C

193302127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29083735-G-A

193302585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29084208-C-T

193302648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29084261-C-T

193302726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29084340-T-C

193302763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29084376-C-G

193302948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29084573-G-A

193302993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29084615-C-T

193304343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29084713-A-G

http://identifiers.org/hco/3/GRCh38#193304676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29085014-C-A

193305175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29085141-T-C

193305221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29085189-T-C

http://identifiers.org/hco/3/GRCh38#193305296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29085259-A-C

193305362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29085499-C-T

193305416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29085556-G-A

193305416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29085556-G-C

193305416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29085556-G-T

http://identifiers.org/hco/3/GRCh38#193305417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29085557-C-A

193305417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29085557-C-T

193305493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29085636-T-A

193305493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29085636-T-C

193305545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29085686-A-G

193305545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29085686-A-T

193305698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29085834-G-T

http://identifiers.org/hco/3/GRCh38#193305835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29085962-A-C

193306165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29092932-G-T

193306335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29093099-T-C

193306640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29093493-T-C

193307092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29093944-A-G

193307127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29093973-T-G

193307152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29093999-T-C

http://identifiers.org/hco/3/GRCh38#193307155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29094002-C-A

193307171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29094008-G-A

193307171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29094008-G-T

193307228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29094053-G-A

193307466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29094303-T-A

193307470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29094307-T-C

193307474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29094311-T-G

http://identifiers.org/hco/3/GRCh38#193307478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29094315-C-A

193307535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29094367-G-A

193307535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29094367-G-C

193308719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29095110-G-A

193309301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29095655-A-G

193309484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29095837-A-G

193309657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096030-G-C

193310767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096531-T-G

193310833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096584-A-G

193310836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096587-T-A

193310856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096608-A-G

193310858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096610-G-A

193310858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096610-G-T

193310880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096631-T-C

193310880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096631-T-G

193310936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096685-G-A

193311206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096955-A-G

193311219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096968-T-A

http://identifiers.org/hco/3/GRCh38#193311232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29096981-C-A

193311284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29097043-T-G

193311619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29097420-G-A

193311626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29097427-C-T

http://identifiers.org/hco/3/GRCh38#193311671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29097473-C-A

http://identifiers.org/hco/3/GRCh38#193311677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29097479-C-A

193311677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29097479-C-G

193311916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29098006-C-G

193311916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29098006-C-T

193311984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29098074-G-A

193311984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29098074-G-C

193311984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29098074-G-T

193311999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29098087-T-C

193312014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29098102-G-A

193312014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29098102-G-C

193312016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29098104-A-G

193312025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29098113-A-T

193312027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29098115-G-T

http://identifiers.org/hco/3/GRCh38#193312051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29098139-C-A

http://identifiers.org/hco/3/GRCh38#193312088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29098176-C-A

http://identifiers.org/hco/3/GRCh38#193312213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29098281-C-A

193312441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29098476-C-T

193312447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29098483-A-G

193313245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099177-G-A

193313245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099177-G-T

193313307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099220-G-A

193313307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099220-G-T

193313425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099319-T-C

193313443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099328-C-T

http://identifiers.org/hco/3/GRCh38#193313496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29099380-C-A

193313496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099380-C-T

http://identifiers.org/hco/3/GRCh38#193313558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29099439-C-A

193313558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099439-C-T

http://identifiers.org/hco/3/GRCh38#193313826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29099531-C-A

193313826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099531-C-T

193313940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099657-A-G

193313942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099659-A-G

193314030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099745-C-T

http://identifiers.org/hco/3/GRCh38#193314240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29099925-C-A

193314240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099925-C-T

193314252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099937-C-T

193314270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099955-A-T

193314296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29099980-T-C

193314514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29100184-G-A

193314744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29100581-G-A

193314769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29100600-G-A

193314778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29100609-C-G

193314778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29100609-C-T

193314887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29100693-A-T

193314888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29100694-T-A

193314888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29100694-T-C

193314895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29100701-A-G

http://identifiers.org/hco/3/GRCh38#193314985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29100775-A-C

193314985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29100775-A-T

193315003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29100793-A-G

193315081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29100871-T-C

193315081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29100871-T-G

193315106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29100896-C-G

193315129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29100921-A-G

193315229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29101023-A-G

193315229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29101023-A-T

193315347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29101119-G-A

193315414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29101173-T-C

193316893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29108083-A-G

193317334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29108492-A-T

193317336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29108494-T-C

193317418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29108579-C-T

http://identifiers.org/hco/3/GRCh38#193317430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29108589-A-C

193317430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29108589-A-G

193317518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29108668-T-C

193317620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29108764-G-A

193317634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29108780-C-T

193317713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29108854-G-C

http://identifiers.org/hco/3/GRCh38#193317916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29109046-C-A

193317966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29109097-C-G

193318072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29109199-C-G

http://identifiers.org/hco/3/GRCh38#193318174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29109288-C-A

193318203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29109312-T-A

193318203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29109312-T-C

193318279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29111597-C-G

http://identifiers.org/hco/3/GRCh38#193318317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29111635-C-A

193318449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29111752-T-A

193318747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29112003-G-A

193318756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29112015-G-A

193318870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29112118-A-G

http://identifiers.org/hco/3/GRCh38#193319190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29112442-C-A

193319190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29112442-C-G

193319194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29112446-G-T

193319221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29112467-T-C

193319328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29112557-G-A

193319767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29112981-G-A

193319960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29113168-C-T

193320038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29113599-A-G

193320074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29113634-T-G

193320149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29113717-A-G

193320465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29113932-G-A

193320539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29113991-G-A

193320723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29114265-T-C

193321326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29116082-G-C

193321659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29116149-T-C

193321659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29116149-T-G

http://identifiers.org/hco/3/GRCh38#193321750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/16/GRCm39#29116266-C-A

193321750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29116266-C-T

193321966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29116482-T-A

193322307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29116793-G-A

193322307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29116793-G-C

193322424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29116919-G-T

193322460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29116955-G-A

http://identifiers.org/hco/3/GRCh38#193322688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29117181-C-A

193322842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29117330-T-A

193323016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29117466-T-C

193323060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29117510-G-T

193323072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29117522-T-C

193323076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29117526-A-G

193323321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29117631-C-T

193323323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29117633-C-T

193323432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29117732-G-T

193323469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29117765-G-A

193323469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29117765-G-T

193323543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29117829-G-C

http://identifiers.org/hco/3/GRCh38#193323569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29117855-C-A

193323569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29117855-C-T

193323583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29117869-A-T

193323584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29117870-A-T

http://identifiers.org/hco/3/GRCh38#193323594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29117880-C-A

193323594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29117880-C-T

http://identifiers.org/hco/3/GRCh38#193323638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29117924-C-A

193323643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29117930-T-A

193323663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29117950-C-G

193323797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29118092-G-C

193323797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29118092-G-T

193323857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29118150-C-G

193323857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29118150-C-T

193324020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29118813-G-A

193324076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29118864-T-A

193324119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29118909-G-T

193324154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29118938-G-A

193324173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29118952-A-G

193324305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29119092-C-T

http://identifiers.org/hco/3/GRCh38#193324359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29119146-A-C

193324520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29119272-A-G

193324566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29119316-C-T

193324767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29126928-G-A

193324767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29126928-G-T

193324788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29126949-A-T

193324844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29127002-C-T

193325031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29127189-T-C

193325312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29127982-T-C

193325494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29128163-A-G

193325573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29128176-T-A

193325573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29128176-T-C

193325644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29128258-G-A

193325743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29128365-C-G

193325881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29128502-A-G

193325961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29128580-G-C

193325972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29128591-G-A

193325975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29128594-A-T

193326340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29128890-C-G

193326438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29128989-A-G

193326566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29129116-T-C

193326582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29129132-A-T

193326763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29129348-A-G

193326872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29129461-A-T

http://identifiers.org/hco/3/GRCh38#193326920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29129483-C-A

193326932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29129495-G-T

193326941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29129504-T-A

193327103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29129662-T-A

193327103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29129662-T-C

193327149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29129704-A-G

193327149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29129704-A-T

193327278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29129773-A-T

193327291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29129781-G-A

193327368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29129869-T-C

http://identifiers.org/hco/3/GRCh38#193327519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29130023-A-C

193327519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29130023-A-T

193327520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29130024-G-A

193327730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29130217-T-G

193327804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29130280-G-A

http://identifiers.org/hco/3/GRCh38#193327819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29130295-C-A

193327881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29130337-C-T

193327958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29130400-C-T

193328320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29130734-A-G

193328328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29130740-G-A

193328363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29130773-G-A

193328363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29130773-G-C

193328486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29130904-C-G

193328486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29130904-C-T

193328521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29130944-T-G

193328650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29131085-T-A

193328796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29131202-A-G

193329300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29131371-C-T

193329462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29131523-C-T

193329602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29131636-T-G

193329762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29131830-G-A

193329765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29131833-G-A

193330100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29132328-C-T

193330215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29132404-G-A

193330286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29132480-T-C

193330355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29132547-T-C

193330361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29132553-G-A

193330585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29132773-C-T

193330799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29133012-G-A

http://identifiers.org/hco/3/GRCh38#193330975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29133177-C-A

193330975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29133177-C-T

193330984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29133186-G-A

193330984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29133186-G-T

http://identifiers.org/hco/3/GRCh38#193330985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29133187-C-A

193331004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29133206-T-C

193331177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: synonymous variant
orthologous variants: 29133378-G-A

193331194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: missense variant
orthologous variants: 29133395-T-C

193331216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: synonymous variant
orthologous variants: 29133417-A-G

193331252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: synonymous variant
orthologous variants: 29133453-T-C

http://identifiers.org/hco/3/GRCh38#193331261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29133462-A-C

193331339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29133539-G-T

http://identifiers.org/hco/3/GRCh38#193331350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29133550-C-A

193331350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29133550-C-G

193331396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29133699-G-T

193331411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29133713-G-A

193331411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29133713-G-T

193331419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29133721-G-A

193331419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29133721-G-C

193331487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29133806-C-T

193331543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29133922-C-T

193332671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29134209-A-G

193332769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29134306-A-G

193333272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29134717-A-G

193333349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29134796-C-T

193333367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29134814-A-G

193333422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29134865-G-A

193333643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29135350-G-A

193333643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29135350-G-T

193333651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29135358-G-T

http://identifiers.org/hco/3/GRCh38#193333674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29135381-C-A

193333674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29135381-C-G

193333674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29135381-C-T

193333794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, missense_variant
orthologous variants: 29135498-C-T

193334103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29139499-G-A

193334251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29139648-G-A

193334518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29140096-C-T

193334798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29140310-G-A

193334798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29140310-G-T

193334802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29140314-G-C

193334802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29140314-G-T

http://identifiers.org/hco/3/GRCh38#193334829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29140342-C-A

193334829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29140342-C-T

193334883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29140396-C-G

193334883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29140396-C-T

193334886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29140399-T-C

193334923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29140435-A-G

193335479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29140911-T-C

193335719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29141742-C-T

193335834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29141857-T-C

193335836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29141859-C-T

193336056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29142110-A-G

193339492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29142333-A-G

193339506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29142347-A-G

193339693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29142539-C-T

193339756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29142603-G-C

193340201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29143013-A-G

193340242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29143054-T-C

193340351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29143159-G-A

193340351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29143159-G-T

http://identifiers.org/hco/3/GRCh38#193340465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29143261-A-C

193340562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29143356-G-A

193341069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29143768-A-T

http://identifiers.org/hco/3/GRCh38#193341165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29143840-C-A

193341465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29144138-G-A

193341877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29144425-A-G

193341880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29144428-T-C

http://identifiers.org/hco/3/GRCh38#193342145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29144672-A-C

http://identifiers.org/hco/3/GRCh38#193342282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29144806-C-A

193342549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29145081-A-G

193342772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29145256-C-T

193342954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29145402-A-G

193343012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29145465-T-C

193343410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29145994-A-G

193343426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146010-C-T

193343427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146011-G-A

193343427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146011-G-T

http://identifiers.org/hco/3/GRCh38#193343440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29146024-C-A

193343440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146024-C-G

193343440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146024-C-T

193343566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146130-A-G

193343566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146130-A-T

193343620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146183-T-G

193343667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146226-T-C

193343702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146260-T-C

193343771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146327-G-C

193343771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146327-G-T

193343801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146356-G-A

193343801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146356-G-T

193343805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146360-G-T

http://identifiers.org/hco/3/GRCh38#193343807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29146362-C-A

193343807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146362-C-T

193343815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146370-C-T

193343869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146422-T-C

193343877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146429-T-C

193343877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146429-T-G

193343919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 29146477-C-T

193344015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 29146573-G-A

193344114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146674-G-A

http://identifiers.org/hco/3/GRCh38#193344157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29146725-C-A

193344371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146939-G-A

193344416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29146966-G-A

193344862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29147364-G-A

193344862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29147364-G-C

193344862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29147364-G-T

193344863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29147365-G-A

193344863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29147365-G-T

193344871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29147375-T-C

193344914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29147417-A-G

http://identifiers.org/hco/3/GRCh38#193344957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29147441-C-A

193344957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29147441-C-T

193345143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29147613-C-G

193345143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29147613-C-T

193345208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29147680-T-A

193345208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29147680-T-C

193346325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29148389-A-G

193346361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29148423-T-C

193346373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29148434-G-A

193346599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29148678-T-C

http://identifiers.org/hco/3/GRCh38#193346674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29148754-A-C

193346758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29148828-T-C

http://identifiers.org/hco/3/GRCh38#193346759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29148829-A-C

193346817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29148886-G-A

193346817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29148886-G-T

193346894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29148963-T-C

193346998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29149048-G-C

193347061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29149133-C-T

193347090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29149160-C-T

193347744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29149962-G-A

193347877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29150095-G-A

193347930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29150139-G-A

193348050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29150253-A-T

193348154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29150355-G-A

193348581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29150782-G-C

193348905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29151035-G-A

193349289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29151346-C-T

193350742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29152445-A-T

193350748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29152451-C-T

http://identifiers.org/hco/3/GRCh38#193350985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29152678-C-A

193350985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29152678-C-T

193351011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29152704-G-A

193351011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29152704-G-T

193351172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: synonymous variant
orthologous variants: 29152871-G-A

193351196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: missense variant
orthologous variants: 29152895-T-A

193351196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: synonymous variant
orthologous variants: 29152895-T-C

193351205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 29152904-C-T

193351364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29153042-G-A

193351757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29154099-C-T

193351837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29154172-C-T

193351838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29154173-A-G

193352026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29154695-A-G

193352185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29154855-A-G

193352528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29155223-A-T

193352579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29155271-G-A

193352949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29155863-T-A

193352980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29155899-C-T

193353094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29156015-A-G

193353105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29156026-G-A

http://identifiers.org/hco/3/GRCh38#193353336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29156272-C-A

193353336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29156272-C-T

193353343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29156277-G-A

http://identifiers.org/hco/3/GRCh38#193353379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29156306-A-C

193353379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29156306-A-T

193353452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29156361-T-A

193353511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29156419-T-A

http://identifiers.org/hco/3/GRCh38#193354061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29157772-C-A

193354061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29157772-C-T

193354064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29157783-G-A

193354064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29157783-G-C

193354064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29157783-G-T

193354151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: synonymous variant
orthologous variants: 29157867-G-A

193354174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: missense variant
orthologous variants: 29157890-C-T

193354236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29157951-G-A

193354236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29157951-G-T

193354238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29157953-A-G

193354248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29157964-T-A

193354294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29158013-G-T

193354295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29158014-A-T

193354366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29158076-A-G

http://identifiers.org/hco/3/GRCh38#193354405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29158119-A-C

193354495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29158197-T-C

193354619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29158313-G-A

193354619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29158313-G-T

193354940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29158603-C-T

193355383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29158678-A-G

193355383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29158678-A-T

http://identifiers.org/hco/3/GRCh38#193355413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29158708-A-C

193355687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29158971-C-G

193355687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29158971-C-T

193355719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29159002-C-T

193355819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29159078-A-G

193355873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29159128-C-T

193355965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29159219-C-T

http://identifiers.org/hco/3/GRCh38#193356057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29159322-C-A

http://identifiers.org/hco/3/GRCh38#193356246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29159528-C-A

193356618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29160077-T-C

193357054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29160345-T-C

193357079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29160356-G-C

193357335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29160576-G-A

193357335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29160576-G-C

193357350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29160591-T-C

http://identifiers.org/hco/3/GRCh38#193357804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29161050-C-A

193357846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29161093-C-T

193358608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29163656-A-G

193358641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29163688-C-T

193358721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29163752-C-G

193358721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29163752-C-T

http://identifiers.org/hco/3/GRCh38#193358842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29163874-A-C

http://identifiers.org/hco/3/GRCh38#193359121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29164135-C-A

193359121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29164135-C-T

193359141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29164155-G-A

http://identifiers.org/hco/3/GRCh38#193359427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29164451-C-A

193359578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29164589-A-G

http://identifiers.org/hco/3/GRCh38#193359596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29164607-C-A

193359596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29164607-C-T

193359634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29164645-C-T

193359987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29164883-T-C

193360347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29165198-A-G

193360498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29165356-C-G

193360498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29165356-C-T

193360548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29165404-T-A

193361500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29166235-T-G

193361526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29166261-G-A

193361529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29166264-G-A

193361539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29166267-G-T

193361580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29166308-G-A

193361580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29166308-G-T

193361609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29166336-A-G

193361790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29166757-C-G

193362049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29167024-C-G

193362049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29167024-C-T

193362230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29167174-G-A

193362230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29167174-G-T

http://identifiers.org/hco/3/GRCh38#193362244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29167185-A-C

193362258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29167201-T-A

http://identifiers.org/hco/3/GRCh38#193362307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29167240-C-A

193362307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29167240-C-T

193362321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29167254-G-T

193362543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29167470-G-A

193362543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29167470-G-T

193362545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29167472-G-A

193362679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29167606-T-A

http://identifiers.org/hco/3/GRCh38#193363143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29167680-A-C

193363153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29167690-T-C

193363194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29167730-C-T

193363279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: missense variant
orthologous variants: 29167817-C-T

http://identifiers.org/hco/3/GRCh38#193363489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29167945-A-C

193363489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29167945-A-G

193363723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29168297-G-C

193363835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29168407-T-C

193363884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29168456-C-G

193363932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29168502-C-T

193364209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: synonymous variant
orthologous variants: 29169556-C-T

193364318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29169660-T-A

193364318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29169660-T-C

193364389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29169726-A-T

193364560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29169885-G-T

193365525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29181433-T-C

193365544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29181448-T-C

193365555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29181459-T-C

193365761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29181648-T-C

193365982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29181867-A-G

193366003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29181888-A-G

193366292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29182208-G-A

193366320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29182234-T-C

http://identifiers.org/hco/3/GRCh38#193366356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29182270-A-C

193366391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29182305-G-C

193369597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29188021-G-C

http://identifiers.org/hco/3/GRCh38#193370519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29188823-C-A

193370945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29191038-C-T

193372585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29191589-C-G

193372630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29191624-C-T

193372769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29191765-A-T

193372941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29191917-A-G

193373046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29192006-G-A

193373514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29192146-T-C

http://identifiers.org/hco/3/GRCh38#193373584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29192215-C-A

193373646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29192254-C-T

193373737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29192332-G-A

http://identifiers.org/hco/3/GRCh38#193373808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29192400-C-A

193373808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29192400-C-T

193373855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29192438-G-A

193374020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29192596-G-A

http://identifiers.org/hco/3/GRCh38#193374085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29192661-A-C

193375325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29194364-C-G

193375336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29194375-C-G

193375403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29194430-T-G

193375774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29194812-G-C

193376037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29195069-G-A

193376895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29195448-C-G

193377105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29195685-A-G

193377135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29195699-G-A

193377135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29195699-G-C

193377168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29195731-A-G

193377168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29195731-A-T

193377338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29195907-C-T

193377398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29195966-T-C

193377518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29196136-A-T

193377559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29196179-G-T

193377708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29196309-G-A

193377937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29196536-G-C

193378238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29196830-C-G

193378305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29196902-T-C

http://identifiers.org/hco/3/GRCh38#193378561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29197207-C-A

193378561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29197207-C-G

193378561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29197207-C-T

193378586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: intron variant
orthologous variants: 29197227-T-C

193378751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 5 prime UTR variant
orthologous variants: 29197380-T-C

193378788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31789
most severe consequence: 5 prime UTR variant
orthologous variants: 29197416-G-T