116877237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non coding transcript exon variant
orthologous variants: 51553870-G-A

116877237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non coding transcript exon variant
orthologous variants: 51553870-G-T

116877257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51553888-G-A

116877257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51553888-G-T

http://identifiers.org/hco/6/GRCh38#116877261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51553891-C-A

116877261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51553891-C-T

116877294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51553924-C-T

http://identifiers.org/hco/6/GRCh38#116877367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51553997-A-C

116877367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51553997-A-T

116877401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51554031-A-T

116877428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51554056-G-A

116877428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51554056-G-T

http://identifiers.org/hco/6/GRCh38#116877452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51554079-C-A

116877452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51554079-C-T

116877455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51554082-G-A

116877455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51554082-G-T

116877458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51554085-G-A

116877458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51554085-G-C

116877458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51554085-G-T

116877510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51554137-G-A

116877510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51554137-G-T

116877515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51554141-A-T

116877574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51554189-G-A

116877574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51554189-G-T

116877999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51554575-A-G

116878005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51554581-A-G

116878006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51554582-G-A

http://identifiers.org/hco/6/GRCh38#116878029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51554605-C-A

116878035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51554611-T-A

116878108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51554679-A-G

116878503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51554996-G-A

116878503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51554996-G-T

116878654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51555148-T-C

http://identifiers.org/hco/6/GRCh38#116878690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51555184-C-A

116878823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51555307-T-G

116878880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51555358-A-T

http://identifiers.org/hco/6/GRCh38#116878994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51555471-C-A

116879340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51555915-T-C

116879681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51556428-G-A

116879733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51556480-G-T

116879975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51556702-C-T

116879983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51556710-A-G

116879994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51556719-G-C

116880028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51556750-A-G

116880249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51556951-G-C

116880277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51556984-C-T

116880389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51557100-G-T

http://identifiers.org/hco/6/GRCh38#116880441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51557804-C-A

116880441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51557804-C-T

http://identifiers.org/hco/6/GRCh38#116880480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51557843-C-A

116880480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51557843-C-G

116880513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51557875-A-G

116880658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51558020-C-T

116880673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51558035-T-C

116880699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51558061-T-A

116880699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51558061-T-C

116880705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51558067-A-T

116880728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51558087-G-A

116880728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51558087-G-T

116880744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51558103-G-A

116880776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51558135-T-G

http://identifiers.org/hco/6/GRCh38#116880822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51558175-A-C

116880822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51558175-A-G

116880849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51558208-T-A

116880855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51558214-C-T

116881180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51558519-T-C

116881197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51558525-G-A

116881197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51558525-G-T

116881987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51559437-C-T

http://identifiers.org/hco/6/GRCh38#116882088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51559537-A-C

116882218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51559564-A-T

116882329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51559647-T-C

116882576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51559865-A-G

116882576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51559865-A-T

116882577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51559866-A-G

116882580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51559869-A-T

116882727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51559916-G-A

116882905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51560075-A-G

http://identifiers.org/hco/6/GRCh38#116882980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51560142-C-A

116883014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51560171-T-C

116883042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51560195-G-A

116883123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51560272-A-G

116883190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51560357-T-G

116883300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51560466-A-T

116883330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51560490-T-C

116883440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51560565-G-C

116883540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51560665-C-T

116883674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51560776-A-G

116884025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51560896-T-C

116884637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51561462-G-T

http://identifiers.org/hco/6/GRCh38#116884742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51561567-C-A

http://identifiers.org/hco/6/GRCh38#116885083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51561896-C-A

116885097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51561910-G-T

116885118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51561930-A-G

116885274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51562056-A-T

116885436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51562226-G-C

116885468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51562273-A-G

116885742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51562538-A-G

116885911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51562695-C-T

116887433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51563230-A-T

116887538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51563318-T-C

116887581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51563354-A-G

116887634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51563396-T-A

116887644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51563406-T-C

116888420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51564158-A-G

116888437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51564182-A-T

116888449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51564194-G-A

116888579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51564332-T-C

116888585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51564337-A-G

116888732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51564453-C-T

116888859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51564575-C-T

116889268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51564985-T-C

116889281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51564998-A-T

http://identifiers.org/hco/6/GRCh38#116889297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51565015-A-C

116889463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51565105-G-C

116889702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51565332-G-A

116889703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51565333-G-A

116890029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51565663-G-T

116890064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51565697-G-A

http://identifiers.org/hco/6/GRCh38#116890481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51566891-A-C

116890536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51566931-G-A

116890536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51566931-G-T

116890553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51566948-C-T

116890574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51566969-T-A

116890574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51566969-T-C

116891134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51567378-G-C

116891336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51567568-A-G

116891493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51567728-G-A

116891763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51568004-T-C

116891863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51568096-T-A

116891892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51568123-T-C

http://identifiers.org/hco/6/GRCh38#116891906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51568137-C-A

116891906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51568137-C-T

116891925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51568157-A-G

116892022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51568254-T-C

116892089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51568287-A-G

116892170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51568366-G-A

116892379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51568506-A-G

116892436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51568558-T-G

116892784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51569372-G-A

116892878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51569464-T-A

116892884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51569470-T-C

116893010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51569543-T-C

116893021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51569554-G-A

116893054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51569587-G-A

116893923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51569743-G-A

116893923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51569743-G-T

http://identifiers.org/hco/6/GRCh38#116893954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51569760-C-A

116893954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51569760-C-G

116893954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51569760-C-T

116893990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51569795-T-C

http://identifiers.org/hco/6/GRCh38#116894056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51569861-C-A

116894056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51569861-C-G

116894056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51569861-C-T

116894120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51569915-T-C

116894120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51569915-T-G

http://identifiers.org/hco/6/GRCh38#116894123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51569918-C-A

116894123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51569918-C-G

116894205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51570001-A-G

116894258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51570058-G-A

116894353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51570362-G-C

116894536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51570540-C-T

116894619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51570618-G-C

116895035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51570998-T-G

116895136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51571054-T-C

116895230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51571144-T-C

116895673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51571559-C-G

116895681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51571625-T-C

116895703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51571734-C-T

116896397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51572414-G-C

http://identifiers.org/hco/6/GRCh38#116898728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51573190-C-A

116898789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51573234-G-A

116898868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51573305-A-G

116898880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51573320-G-A

116899076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51573480-G-A

116899279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51573643-T-G

116902660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51579250-T-C

116902928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51579507-T-C

116902988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51579564-T-C

116903035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51579611-A-G

116903140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51579716-A-G

116903140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51579716-A-T

116903244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51579824-T-G

116903418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51579991-G-A

116903564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51580096-C-T

116903823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51580349-T-C

116903832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51580358-G-A

116903832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51580358-G-C

116903946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51580470-C-T

116909447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51582993-C-G

http://identifiers.org/hco/6/GRCh38#116909464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51583010-C-A

116909656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51583214-G-T

116909698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51583255-A-T

116909766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51583290-A-G

116909766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51583290-A-T

http://identifiers.org/hco/6/GRCh38#116909769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51583293-C-A

116909769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51583293-C-G

116909769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51583293-C-T

116909887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51583328-A-G

116910208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51584004-A-G

116910426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51584223-G-T

116910436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51584233-C-G

116910453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51584250-A-T

116910461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51584260-T-G

116910514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51584315-G-A

116911277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51585015-C-T

116911305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51585044-A-G

116911758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51585424-G-T

116912693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51585913-T-A

116912835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51586026-A-G

116912937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51586120-G-T

116913437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51586398-C-G

116913441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51586402-G-A

http://identifiers.org/hco/6/GRCh38#116913448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51586419-C-A

116913689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51586681-G-C

116914694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51587181-T-C

116914695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51587182-G-T

http://identifiers.org/hco/6/GRCh38#116914771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51587246-C-A

116914853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51587317-C-T

116915799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51587716-A-T

116915873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51587791-A-G

http://identifiers.org/hco/6/GRCh38#116915903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51587820-C-A

116915903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51587820-C-T

116915959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51587872-G-A

116915980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51587881-T-C

116915989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51587890-T-C

116916040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51587941-C-T

http://identifiers.org/hco/6/GRCh38#116916073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51587974-A-C

116916073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51587974-A-T

http://identifiers.org/hco/6/GRCh38#116916119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51588015-A-C

116916124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588020-A-G

116916145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588041-T-G

116916149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588045-T-G

116916193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 51588069-G-C

116916331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588207-G-A

116916335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588211-T-A

116916390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588262-A-G

116916402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588265-T-C

116916460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588277-T-C

116916498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588283-A-G

116916560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588345-C-T

116916689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588460-T-A

116916696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588467-T-G

116916741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588498-T-C

116916906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588645-T-A

116917305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588767-G-A

116917320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588778-G-A

116917357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588812-G-T

http://identifiers.org/hco/6/GRCh38#116917505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51588962-A-C

116917505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51588962-A-T

http://identifiers.org/hco/6/GRCh38#116917541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51589001-C-A

116917676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51589139-G-A

http://identifiers.org/hco/6/GRCh38#116917764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51589199-C-A

116917765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51589200-A-G

116917868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51589268-C-T

116917945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51589338-A-G

116917961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51589354-G-C

116917961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51589354-G-T

116918128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51589659-T-A

116918128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51589659-T-C

116918132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51589663-A-G

116918167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51589696-G-C

116918226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51589745-A-G

116918226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51589745-A-T

116918302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51589830-G-A

116918367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51589907-G-A

http://identifiers.org/hco/6/GRCh38#116918464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51590012-C-A

116918464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51590012-C-T

http://identifiers.org/hco/6/GRCh38#116918577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51590119-C-A

116918577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51590119-C-T

116918673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51590206-G-A

116918793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51590316-G-A

116918998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51591841-G-A

116918998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51591841-G-T

116919009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51591851-G-A

116919203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51592052-C-G

116919260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51592109-T-C

116919302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51592151-T-C

116919391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51592223-G-A

http://identifiers.org/hco/6/GRCh38#116919394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51592226-C-A

116919394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51592226-C-T

116919405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51592237-A-T

http://identifiers.org/hco/6/GRCh38#116919426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51592258-C-A

116919447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51592277-A-G

116919447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51592277-A-T

116919652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51592490-A-G

116920321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51594170-A-G

116920505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51594351-G-A

116920505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51594351-G-T

116920506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51594352-A-G

http://identifiers.org/hco/6/GRCh38#116920507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51594353-C-A

116920508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51594354-A-G

116920508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51594354-A-T

http://identifiers.org/hco/6/GRCh38#116920510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51594356-C-A

116920510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51594356-C-T

116920553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51594395-G-A

116920556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51594398-G-A

116920556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51594398-G-T

116920626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51594458-C-T

116920702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51594630-A-G

116920792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51594841-A-G

116920838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51594881-T-C

116920925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51594969-A-G

116921321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51595348-C-G

116921524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51595549-A-G

116922026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51596027-T-A

116922073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51596074-G-A

116922073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51596074-G-T

116922136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51596137-A-G

116922219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51596214-T-A

116922219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51596214-T-C

116922219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51596214-T-G

116922393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51596847-C-T

116922402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51596856-C-T

http://identifiers.org/hco/6/GRCh38#116922921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51597393-C-A

116922943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51597428-A-T

116922964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51597451-G-C

116922964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51597451-G-T

http://identifiers.org/hco/6/GRCh38#116923019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51597511-C-A

http://identifiers.org/hco/6/GRCh38#116923061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51597551-C-A

116923061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51597551-C-T

http://identifiers.org/hco/6/GRCh38#116923184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51597674-A-C

116923371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51597855-G-A

116923371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51597855-G-T

116923501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51597972-A-G

116923509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51597980-T-A

116923509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51597980-T-C

116923525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51597996-G-A

116923597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51598031-T-C

116923651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51598095-G-T

116923693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51598137-A-G

116923861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51598314-A-G

116924199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51598643-A-G

http://identifiers.org/hco/6/GRCh38#116924591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51599030-C-A

116924591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51599030-C-G

http://identifiers.org/hco/6/GRCh38#116924620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51599059-C-A

116924620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51599059-C-G

116924664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 51599092-A-G

http://identifiers.org/hco/6/GRCh38#116924790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51599218-A-C

116924790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 51599218-A-G

http://identifiers.org/hco/6/GRCh38#116924805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51599232-A-C

116924805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51599232-A-G

116924841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51599267-A-G

116924883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51599304-A-G

116924930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51599345-T-C

116924992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51599407-T-C

116925252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51599641-G-A

116925259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51599648-T-C

http://identifiers.org/hco/6/GRCh38#116925275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51599662-C-A

116925397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51599774-T-C

116925454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 51599830-T-C

116925484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: synonymous variant
orthologous variants: 51599860-G-A

116925520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: synonymous variant
orthologous variants: 51599896-C-T

116925556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: missense variant
orthologous variants: 51599932-C-G

116925556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: synonymous variant
orthologous variants: 51599932-C-T

116925608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: missense variant
orthologous variants: 51599984-C-T

116925696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51600085-T-A

116925724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51600112-T-A

http://identifiers.org/hco/6/GRCh38#116925765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51600141-A-C

116925780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51600219-T-A

116925780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51600219-T-C

116925831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51600291-A-G

116925838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51600301-T-A

http://identifiers.org/hco/6/GRCh38#116925866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51600325-C-A

116925893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51600350-A-G

116926001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51600439-G-C

116926468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51600895-T-C

116926525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51600951-C-G

116926758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51601165-T-C

116926758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51601165-T-G

116926903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51601340-T-G

116927001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51601437-A-G

116927232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: synonymous variant
orthologous variants: 51601668-T-C

http://identifiers.org/hco/6/GRCh38#116927317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51601753-C-A

116927317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: missense variant
orthologous variants: 51601753-C-G

116927317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: stop gained
orthologous variants: 51601753-C-T

116927436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: synonymous variant
orthologous variants: 51601872-T-C

116927579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51602015-G-A

116927605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51602041-G-A

116927605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51602041-G-C

116927605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51602041-G-T

116928097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51602273-T-A

116928097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51602273-T-C

116928227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51602345-C-G

116928325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51602409-C-T

116928453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51602546-A-G

116928584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51602610-A-G

116928612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51602639-A-G

116928674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51602693-T-A

116928823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: missense variant
orthologous variants: 51602842-C-G

116928823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: synonymous variant
orthologous variants: 51602842-C-T

http://identifiers.org/hco/6/GRCh38#116928871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51602890-C-A

116928871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: synonymous variant
orthologous variants: 51602890-C-T

116928903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: missense variant
orthologous variants: 51602922-G-A

116929022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51603029-A-T

116929048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51603060-T-G

116929051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51603063-G-A

116929051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51603063-G-T

http://identifiers.org/hco/6/GRCh38#116929052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51603064-C-A

116929052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51603064-C-T

116929332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51603316-G-T

116929370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51603355-A-G

116929425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51603412-G-A

116929667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51603832-C-G

116929667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51603832-C-T

116930238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51604405-A-G

116930270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51604440-G-C

116930420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51604582-T-C

http://identifiers.org/hco/6/GRCh38#116930603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51605009-C-A

116930874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51605411-A-G

116930880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51605417-T-C

116930888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51605425-G-A

116930888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51605425-G-T

http://identifiers.org/hco/6/GRCh38#116930918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51605454-A-C

116930918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51605454-A-G

116930938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51605474-G-A

116931173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51605645-G-A

http://identifiers.org/hco/6/GRCh38#116931182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51605654-A-C

116931199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51605671-T-C

http://identifiers.org/hco/6/GRCh38#116931312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51605710-A-C

116931315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: intron variant
orthologous variants: 51605711-A-T

116931546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: 51605935-A-G

116931546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: 51605935-A-T

116931547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: 51605936-T-C

http://identifiers.org/hco/6/GRCh38#116931580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51605970-C-A

116931580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: 51605970-C-G

116931580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: 51605970-C-T

116931586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: 51605976-T-C

http://identifiers.org/hco/6/GRCh38#116931587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51605977-A-C

116931587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: 51605977-A-G

116931597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: 51605987-A-G

116931687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: 51606069-A-G

http://identifiers.org/hco/6/GRCh38#116931716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51606098-C-A

116931725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: 51606107-T-C

116931725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: 51606107-T-G

http://identifiers.org/hco/6/GRCh38#116931734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#51606116-C-A

116931734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21478
most severe consequence: 3 prime UTR variant
orthologous variants: 51606116-C-T