13569216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3 prime UTR variant
orthologous variants: 41945395-G-C

13569216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3 prime UTR variant
orthologous variants: 41945395-G-T

13569220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3 prime UTR variant
orthologous variants: 41945399-T-C

13569423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3 prime UTR variant
orthologous variants: 41945584-G-A

13569746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3 prime UTR variant
orthologous variants: 41945915-G-T

http://identifiers.org/hco/4/GRCh38#13569843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41946010-C-A

13569843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41946010-C-T

13569904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41946071-C-T

13569919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41946086-T-C

13570041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41946205-C-G

13570131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41946295-G-A

13570248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41946393-T-A

13570248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41946393-T-C

13571144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41947657-T-G

13571240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41947748-C-G

13571275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41947783-A-G

13571417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41947919-G-A

13571431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41947946-A-G

13571432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41947947-T-C

13571499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41948008-T-C

13571579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41948096-C-T

13571857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41948319-G-T

13572067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41948490-A-G

13572197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41948651-T-C

13572600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41949059-T-C

13573087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41949510-G-T

13573195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41949609-G-A

http://identifiers.org/hco/4/GRCh38#13574002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41949846-A-C

http://identifiers.org/hco/4/GRCh38#13574050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41949886-A-C

13574050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41949886-A-G

13574079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41949908-A-G

13574143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41949967-C-T

13574153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41949977-G-A

http://identifiers.org/hco/4/GRCh38#13574237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41950055-C-A

13574806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41950660-G-A

13576227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951111-T-C

http://identifiers.org/hco/4/GRCh38#13576662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41951424-A-C

13576750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951482-G-A

13576750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951482-G-C

13576750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951482-G-T

13576826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951558-T-C

13576873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41951605-G-C

13576939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41951671-C-T

13577051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951783-G-A

13577051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951783-G-C

13577051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951783-G-T

13577063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951793-G-A

13577063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951793-G-C

13577063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951793-G-T

13577123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951852-G-T

13577188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951917-T-A

13577188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41951917-T-G

13577390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41952212-G-C

13577390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41952212-G-T

13577602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 41952433-G-A

13577602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41952433-G-T

13579395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41954579-T-C

13579579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41954757-A-G

13580057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41955493-G-A

13580057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41955493-G-T

13580314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41955738-T-C

13580315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41955739-A-G

13580352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41955782-T-G

http://identifiers.org/hco/4/GRCh38#13580816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41956907-A-C

13580860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41956948-T-C

http://identifiers.org/hco/4/GRCh38#13580883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41956975-A-C

13580883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41956975-A-G

13580948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957050-T-G

13580951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957053-A-G

http://identifiers.org/hco/4/GRCh38#13581025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41957120-C-A

13581025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41957120-C-T

13581029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41957124-G-A

13581029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41957124-G-C

13581029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41957124-G-T

13581113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957214-A-G

http://identifiers.org/hco/4/GRCh38#13581120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41957221-C-A

13581120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957221-C-T

13581144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41957245-T-C

http://identifiers.org/hco/4/GRCh38#13581199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41957300-C-A

13581199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41957300-C-T

13581216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957317-G-A

13581216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957317-G-C

13581216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957317-G-T

13581326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957409-T-G

13581329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957415-G-A

13581417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957482-T-C

13581606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957633-G-A

13581875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957847-C-G

13581988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957904-C-G

13582086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957977-T-A

13582086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957977-T-C

13582093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41957984-T-C

http://identifiers.org/hco/4/GRCh38#13582210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41958076-C-A

http://identifiers.org/hco/4/GRCh38#13582227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41958093-C-A

13582227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41958093-C-T

13582253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41958119-G-A

13582356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41958224-G-T

13582367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41958235-C-G

13582367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41958235-C-T

13582381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41958246-C-G

13582381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41958246-C-T

http://identifiers.org/hco/4/GRCh38#13582445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41958310-C-A

13582445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41958310-C-T

13582459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41958324-G-T

http://identifiers.org/hco/4/GRCh38#13582536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41958382-C-A

13582607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41958461-G-T

13582618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41958472-T-C

13582619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41958473-C-T

13582622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41958476-T-C

http://identifiers.org/hco/4/GRCh38#13582681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41958528-C-A

13582681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41958528-C-G

13582681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41958528-C-T

http://identifiers.org/hco/4/GRCh38#13582758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41958605-C-A

13582758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41958605-C-T

13582774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41958624-A-T

13583071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41959289-G-A

13583092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41959307-T-A

13583133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41959348-G-A

13583810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41960792-G-C

13584067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41961003-G-T

13584275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41961197-A-G

13584283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41961205-T-C

13584680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41961406-C-G

13584802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41961525-T-C

13585047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41961791-T-C

http://identifiers.org/hco/4/GRCh38#13585227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41961966-C-A

13585392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41962072-G-A

http://identifiers.org/hco/4/GRCh38#13586250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41962379-C-A

http://identifiers.org/hco/4/GRCh38#13586348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41962462-C-A

13586348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41962462-C-T

13586399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41962498-T-A

http://identifiers.org/hco/4/GRCh38#13586429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41962528-C-A

13586440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41962539-T-C

http://identifiers.org/hco/4/GRCh38#13586541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41962637-C-A

13586560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41962653-G-A

13586560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41962653-G-T

http://identifiers.org/hco/4/GRCh38#13586596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41962689-A-C

13586748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41963021-A-T

13587199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41963580-C-T

13587421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41963782-G-A

http://identifiers.org/hco/4/GRCh38#13587684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41964019-C-A

13587690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41964023-T-A

13587700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 41964033-T-A

13587700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 41964033-T-C

13587700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 41964033-T-G

13587709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41964042-T-A

http://identifiers.org/hco/4/GRCh38#13587727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41964060-C-A

13587727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41964060-C-T

13588593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41964385-T-A

13588593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41964385-T-C

http://identifiers.org/hco/4/GRCh38#13588655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41964447-C-A

13588655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41964447-C-T

13588801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41964595-T-A

13588864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41964660-G-A

13588864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41964660-G-C

13588864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41964660-G-T

13589091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41964842-T-C

http://identifiers.org/hco/4/GRCh38#13589092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41964843-C-A

13589092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41964843-C-G

13589092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41964843-C-T

13589233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41964981-C-G

http://identifiers.org/hco/4/GRCh38#13589443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41965173-C-A

13589444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41965174-A-G

http://identifiers.org/hco/4/GRCh38#13590235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41965897-C-A

13590235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41965897-C-T

13590270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41965929-T-A

13590351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41966012-T-C

http://identifiers.org/hco/4/GRCh38#13590404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#41966065-C-A

13590404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41966065-C-G

13590404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41966065-C-T

13590409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41966070-T-A

13590409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41966070-T-C

13590409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41966070-T-G

13590438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41966099-A-G

13590463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41966124-A-G

13590546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41966196-T-C

13590653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41966302-G-T

13590799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41966442-C-T

13590968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41966516-G-A

13591021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41966571-C-T

13591090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41966623-A-G

13591291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41966816-T-C

13591338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41966870-G-A

13591338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41966870-G-C

13591505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41967032-G-T

13591546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41967068-G-A

13591567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41967089-G-C

13591570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41967092-A-G

13591627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41967134-C-T

13591949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41967424-G-A

13591949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41967424-G-T

13592053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41967520-G-C

13592053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41967520-G-T

13592098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41967565-A-G

13592251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41967687-G-A

13592251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41967687-G-T

13592719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41968112-G-T

13592832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41968220-G-A

13592832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41968220-G-T

13594440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41968957-G-T

13595390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41969783-T-C

13595513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41969875-C-T

13595528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41969890-C-G

13595573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41969935-T-C

13595615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41969974-C-T

http://identifiers.org/hco/4/GRCh38#13595776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41970370-C-A

13595776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41970370-C-T

13595885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41970490-C-T

13595894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41970499-T-C

http://identifiers.org/hco/4/GRCh38#13595944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41970549-C-A

13595995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41970587-A-G

http://identifiers.org/hco/4/GRCh38#13596174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41970756-A-C

13596409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41970958-T-C

13596872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41971365-T-G

13596879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41971372-G-A

13597256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41971623-G-T

13597307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41971674-T-C

13597336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41971728-A-G

13597642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41972047-G-C

http://identifiers.org/hco/4/GRCh38#13597655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41972064-A-C

13597827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41972281-G-T

13598077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41973015-G-A

13598274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41973227-T-C

13598609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41973355-T-C

13598716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41973462-T-A

13599031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41973636-T-A

13599031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41973636-T-G

13599045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41973650-C-T

13599378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41973956-G-A

13599378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41973956-G-C

http://identifiers.org/hco/4/GRCh38#13599514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#41974101-C-A

13599514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense_variant, undefined
orthologous variants: 41974101-C-G

13599514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous_variant, undefined
orthologous variants: 41974101-C-T

13599587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41974132-C-T

13599719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41974267-T-C

13599830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41974378-G-A

13599913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41974461-G-A

13600009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41974557-G-A

13600075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41974623-C-G

13600075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41974623-C-T

http://identifiers.org/hco/4/GRCh38#13600213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41974737-A-C

13600565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41975086-G-A

13600578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41975099-T-C

13600711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41975229-C-T

13600936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41975430-G-A

13601029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41975523-A-T

13601252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41975743-G-A

13601299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41975790-C-T

http://identifiers.org/hco/4/GRCh38#13601494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41975985-C-A

13601494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41975985-C-T

13601530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41976024-T-C

13601530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41976024-T-G

13601547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41976041-T-G

13601647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41976138-C-T

http://identifiers.org/hco/4/GRCh38#13601675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41976166-C-A

13602183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41976659-G-A

13602389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41976865-T-A

13602403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41976879-G-A

13602482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41976955-A-G

13602748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41977170-C-G

13602748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41977170-C-T

13602872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41977294-C-T

13602888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41977310-G-A

13602888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41977310-G-T

13602975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41977397-C-G

13602975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41977397-C-T

13603006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41977428-T-C

13603117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41977539-A-T

13603163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41977591-G-A

13603371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41977799-T-C

13603546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41977980-C-T

13603667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41978098-A-G

13603948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41978379-T-A

13603948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41978379-T-C

13603971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41978402-C-G

http://identifiers.org/hco/4/GRCh38#13603994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41978425-C-A

13603994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41978425-C-G

13603994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41978425-C-T

13604191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41978622-C-T

13604239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41978670-C-T

13604253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41978684-T-A

13604253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41978684-T-C

http://identifiers.org/hco/4/GRCh38#13604275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41978706-C-A

13604275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41978706-C-G

13604275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41978706-C-T

13604516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41978944-T-C

13604516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41978944-T-G

13604543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41978971-T-A

13604543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41978971-T-C

13604564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41978992-G-C

13604564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41978992-G-T

13604839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41979261-G-A

13604839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41979261-G-C

13604929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41979351-C-T

13604991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41979413-A-T

13605040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41979462-A-G

13605065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: missense variant
orthologous variants: 41979484-A-T

http://identifiers.org/hco/4/GRCh38#13605143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41979550-C-A

13605788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41979938-T-A

13606453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41980305-T-C

13606602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41980447-T-C

13606836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41980662-T-C

13606904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41980731-G-C

http://identifiers.org/hco/4/GRCh38#13606990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41980811-C-A

13606990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41980811-C-T

http://identifiers.org/hco/4/GRCh38#13607049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41980866-A-C

13607049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41980866-A-G

http://identifiers.org/hco/4/GRCh38#13607065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41980885-C-A

13607065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41980885-C-T

13607228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41981425-T-A

13607228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41981425-T-C

13607236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41981433-T-A

13607236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41981433-T-C

13607248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41981445-G-A

13607248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41981445-G-C

13607248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41981445-G-T

13607273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41981461-T-C

13607289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41981477-T-C

13607478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41981623-A-G

http://identifiers.org/hco/4/GRCh38#13608446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41982516-C-A

13608494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41983772-T-C

13608494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41983772-T-G

13608574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41983850-T-C

13608622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: synonymous variant
orthologous variants: 41983898-T-C

http://identifiers.org/hco/4/GRCh38#13608701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41983974-A-C

13608701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41983974-A-G

13608720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41983994-T-A

13608720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41983994-T-C

13609176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41984336-T-A

13609221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41984379-A-G

13609287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 41984444-A-G

13609762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41985136-T-C

13609777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41985150-T-A

13609778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41985151-A-G

13609779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41985152-G-A

13609873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41985207-A-G

13610288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41985612-T-C

13610288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41985612-T-G

13610366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41985687-T-C

13611113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41986275-T-C

13611146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41986305-T-C

13611146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41986305-T-G

13611203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41986368-G-A

13611361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41986474-T-C

13611492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron_variant, undefined
orthologous variants: 41986598-A-G

13611616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41986713-C-G

http://identifiers.org/hco/4/GRCh38#13611890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41987158-A-C

13612006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41987267-C-T

13612066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41987302-G-A

http://identifiers.org/hco/4/GRCh38#13612271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41987506-C-A

13612711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41987872-A-G

13612849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41987988-C-G

13613047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41988185-T-C

13613342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41988622-G-A

13613379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: 41988657-A-G

http://identifiers.org/hco/4/GRCh38#13613472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41988744-A-C

13613585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 41988861-T-C

13613678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41988951-A-G

http://identifiers.org/hco/4/GRCh38#13613712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41988984-C-A

13614171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41989537-T-A

13614384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41989742-T-C

13614438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41989796-C-T

13614495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41989853-T-C

13614495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41989853-T-G

13614518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 41989876-G-A

13614563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41989921-T-A

13614563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 41989921-T-C

13614575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 41989933-G-A

13614575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41989933-G-C

13614672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41990030-G-A

http://identifiers.org/hco/4/GRCh38#13614847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41990566-C-A

13614847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41990566-C-T

13614887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41990606-T-C

13614942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41990643-C-G

13614942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41990643-C-T

13614998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41990696-T-C

http://identifiers.org/hco/4/GRCh38#13615103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41990810-C-A

13615103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41990810-C-T

13615154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41990858-G-A

13615165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41990869-G-T

13615366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41991055-T-C

13615531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41991219-T-C

13615541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41991230-A-G

13615631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41991291-T-A

13615631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41991291-T-C

13616225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41991851-G-T

13617408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41993085-G-T

http://identifiers.org/hco/4/GRCh38#13617887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41993461-A-C

13618240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41994171-A-G

13618511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41994416-G-A

13618898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41994724-A-T

http://identifiers.org/hco/4/GRCh38#13619300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41994859-C-A

13619300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41994859-C-T

13619678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41995124-T-A

13619764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41995227-C-T

http://identifiers.org/hco/4/GRCh38#13619828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41995281-C-A

13619837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41995290-T-C

13619865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41995311-G-T

http://identifiers.org/hco/4/GRCh38#13619917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41995359-C-A

13619917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41995359-C-T

13620112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41995561-T-A

13620112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41995561-T-C

http://identifiers.org/hco/4/GRCh38#13620182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41995630-C-A

13620280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41995713-T-C

http://identifiers.org/hco/4/GRCh38#13620823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41996194-C-A

13620823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41996194-C-T

13620921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41996285-G-T

13621489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41997076-G-A

13621499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41997086-T-C

13621604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41997164-A-G

13622643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41997732-T-C

13622877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41997928-C-T

13623134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41998137-C-G

13623136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41998139-C-T

13623286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41998288-A-G

13623451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41998465-A-G

13623516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41998530-T-C

http://identifiers.org/hco/4/GRCh38#13623727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41998727-C-A

13623933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41998946-G-A

http://identifiers.org/hco/4/GRCh38#13624079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41999057-C-A

13624151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41999119-G-A

13624151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41999119-G-T

13624220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41999140-G-A

13624220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41999140-G-C

13624220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41999140-G-T

13624286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41999183-T-C

13624698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41998673-T-C

13624735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41998710-A-G

http://identifiers.org/hco/4/GRCh38#13624825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41998780-C-A

13624825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41998780-C-T

http://identifiers.org/hco/4/GRCh38#13624853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41998815-C-A

13624958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41998946-G-A

http://identifiers.org/hco/4/GRCh38#13625380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41999375-C-A

13625380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41999375-C-T

13625472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41999463-T-C

http://identifiers.org/hco/4/GRCh38#13625483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41999470-C-A

13625483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 41999470-C-G

http://identifiers.org/hco/4/GRCh38#13625917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#41999877-C-A

13626510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 42000201-G-A

13626520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 42000211-C-T

http://identifiers.org/hco/4/GRCh38#13626536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42000214-C-A

13626537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 42000215-C-T

http://identifiers.org/hco/4/GRCh38#13627257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42001109-C-A

13627257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 42001109-C-T

http://identifiers.org/hco/4/GRCh38#13627320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42001236-C-A

13627320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 42001236-C-T

13627325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 42001241-A-G

http://identifiers.org/hco/4/GRCh38#13627327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42001243-A-C

13627327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 42001243-A-G

http://identifiers.org/hco/4/GRCh38#13627461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42001391-C-A

13627461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 42001391-C-T

http://identifiers.org/hco/4/GRCh38#13627498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#42001428-C-A

13627498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 42001428-C-T

13627522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 42001452-C-T

13627620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 42001544-A-G

13627668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 42001590-G-A

13627668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31792
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 42001590-G-T