43192107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: non coding transcript exon variant
orthologous variants: 120217500-G-A

http://identifiers.org/hco/5/GRCh38#43192129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120217473-C-A

43192129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: non coding transcript exon variant
orthologous variants: 120217473-C-G

43192200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: non coding transcript exon variant
orthologous variants: 120217403-G-T

http://identifiers.org/hco/5/GRCh38#43192234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120217369-C-A

43192234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120217369-C-T

43192244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120217361-T-G

43192258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120217347-G-A

43192362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120217275-C-T

43192363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120217274-C-G

43192363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120217274-C-T

http://identifiers.org/hco/5/GRCh38#43192367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120217270-C-A

43192367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120217270-C-T

43192478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120217163-C-T

43192548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120217116-G-A

43192548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120217116-G-T

43192633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120217043-G-A

43192745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120216968-C-T

43192746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120216967-C-G

43192751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120216966-T-C

http://identifiers.org/hco/5/GRCh38#43192850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120216868-C-A

43192850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120216868-C-T

43192973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120216768-G-A

43192973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120216768-G-T

http://identifiers.org/hco/5/GRCh38#43192974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#120216767-C-A

43192974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120216767-C-T

43193010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120216718-G-A

43193045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120216682-G-T

http://identifiers.org/hco/5/GRCh38#43193128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120216596-C-A

43193128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120216596-C-T

43193139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120216585-A-G

43193140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120216584-G-C

http://identifiers.org/hco/5/GRCh38#43193196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120216545-A-C

http://identifiers.org/hco/5/GRCh38#43193313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120216514-C-A

43193313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120216514-C-T

http://identifiers.org/hco/5/GRCh38#43193373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#120216461-C-A

43193373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120216461-C-T

http://identifiers.org/hco/5/GRCh38#43193421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120216433-A-C

43193421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120216433-A-G

43193432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120216422-C-T

http://identifiers.org/hco/5/GRCh38#43193475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#120216322-C-A

43193914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120215887-A-G

http://identifiers.org/hco/5/GRCh38#43194018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120215776-A-C

43194018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120215776-A-G

43194611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120215188-C-G

43194611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120215188-C-T

http://identifiers.org/hco/5/GRCh38#43195958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120214402-C-A

43206116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209017-C-G

43206216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208947-G-A

http://identifiers.org/hco/5/GRCh38#43208761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120205890-C-A

43208835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205817-A-G

43208844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205808-C-T

43209076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205582-A-G

43209087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205571-C-T

43209115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205543-G-A

43209229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205437-G-A

43209292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205373-T-G

43209348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205316-G-A

43209348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205316-G-T

43209401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205266-T-C

43212711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120204991-C-T

43213893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120204212-T-G

43214178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203990-A-T

43214245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203917-T-C

http://identifiers.org/hco/5/GRCh38#43214399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120203756-C-A

43214433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203710-G-T

43214486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203652-A-G

43215377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203139-T-C

http://identifiers.org/hco/5/GRCh38#43215445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120203013-C-A

43215456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203002-A-G

43225817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120199773-G-C

43225817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120199773-G-T

43225827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120199763-G-C

43226218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120199409-C-T

43226275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120199356-C-T

43226368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120199155-T-C

43226882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198642-G-T

43227751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120197428-C-T

43227844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120197335-T-C

43227998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120197216-T-C

43228075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120197144-A-G

43228612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120196979-C-G

http://identifiers.org/hco/5/GRCh38#43228649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120196927-A-C

43228657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120196919-T-A

43228657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120196919-T-G

http://identifiers.org/hco/5/GRCh38#43228663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120196913-A-C

43228665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120196911-A-T

http://identifiers.org/hco/5/GRCh38#43228672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120196904-A-C

43228685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120196891-G-A

43228689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120196887-G-A

43228689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120196887-G-C

43228957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120196665-T-C

43229019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

43230283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195729-A-G

43230481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195535-G-A

43233422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195329-G-A

43233635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195162-G-C

43233702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195089-G-A

http://identifiers.org/hco/5/GRCh38#43233908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120194791-C-A

43233908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194791-C-G

43234018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194693-T-C

43234211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194526-C-G

43234211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194526-C-T

43236542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193894-G-A

43236634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193803-T-A

43236772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193658-G-C

43236826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193628-A-G

43237070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193396-G-A

43237483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192953-G-A

43237494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192943-A-G

43237496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192941-C-T

43241908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120192088-A-T

43242118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191907-C-T

43242202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191825-C-T

43242205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191822-C-T

43242213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191814-G-C

http://identifiers.org/hco/5/GRCh38#43242413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120191619-C-A

http://identifiers.org/hco/5/GRCh38#43242431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120191600-C-A

43242431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191600-C-T

43242460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191577-G-A

43242783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191290-A-T

43243312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191096-A-G

43243313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191095-G-C

43243946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190613-T-G

43243984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190575-T-C

43244052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190517-T-A

43244117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190468-G-A

43244117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120190468-G-C

http://identifiers.org/hco/5/GRCh38#43244957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120190166-C-A

http://identifiers.org/hco/5/GRCh38#43245047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120190090-C-A

43245167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189964-A-G

43245178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189953-C-T

43245313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189820-G-T

43245323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189810-G-A

43245323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189810-G-T

43245369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189764-G-C

43245369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189764-G-T

43245401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189732-G-A

43245401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189732-G-C

43245401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189732-G-T

43245404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189722-C-T

43245415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189715-C-T

43245481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189672-G-A

43245481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189672-G-T

http://identifiers.org/hco/5/GRCh38#43245517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120189636-C-A

43245536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189624-G-A

43245536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189624-G-T

43245582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189587-T-C

43245633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189548-G-A

43245633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189548-G-T

http://identifiers.org/hco/5/GRCh38#43245639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120189542-C-A

43245639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189542-C-G

43245691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189489-G-A

http://identifiers.org/hco/5/GRCh38#43245701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120189470-C-A

43245701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189470-C-T

http://identifiers.org/hco/5/GRCh38#43245702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120189469-C-A

43245702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189469-C-G

43245706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189465-C-T

http://identifiers.org/hco/5/GRCh38#43245764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120189417-C-A

43245764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189417-C-G

43245764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120189417-C-T

43245790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120189391-T-C

http://identifiers.org/hco/5/GRCh38#43245815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120189366-C-A

43245815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120189366-C-T

http://identifiers.org/hco/5/GRCh38#43245819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120189362-A-C

http://identifiers.org/hco/5/GRCh38#43246058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120189123-C-A

43246058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120189123-C-G

43246617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188948-T-C

43246868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188770-T-C

43246874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188764-A-G

43246914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188739-G-A

43247006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188657-A-G

43247042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188626-G-C

http://identifiers.org/hco/5/GRCh38#43247194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120188444-C-A

43247194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188444-C-T

43247353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188298-T-A

43247412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188231-G-T

http://identifiers.org/hco/5/GRCh38#43247430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120188213-C-A

43247514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120188138-C-G

43250462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120187169-G-A

43250693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186837-T-C

43250836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186703-T-C

43250843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186697-T-A

43250914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186616-A-T

http://identifiers.org/hco/5/GRCh38#43251112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120186452-A-C

43251162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186405-T-C

43251757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183932-C-T

43251812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183881-C-T

http://identifiers.org/hco/5/GRCh38#43251984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120183740-C-A

http://identifiers.org/hco/5/GRCh38#43252327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120183432-A-C

43252387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183378-A-T

43252817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183022-T-C

43252963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120182837-T-C

43253437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120182027-G-C

43253437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120182027-G-T

43253443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120182021-G-A

43253486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181983-T-C

43272803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120180012-A-T

43272827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120179984-G-A

43273018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120179634-C-G

http://identifiers.org/hco/5/GRCh38#43273051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120179601-C-A

43274021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120178781-G-A

43274077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120178531-A-T

43274355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120178283-G-C

43274579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120178082-G-A

43274796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177879-C-T

43274827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177848-C-G

43274891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120177786-A-G

http://identifiers.org/hco/5/GRCh38#43274976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120177718-C-A

43276985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175999-G-T

http://identifiers.org/hco/5/GRCh38#43277030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120175957-C-A

http://identifiers.org/hco/5/GRCh38#43277032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120175955-C-A

43277032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175955-C-T

43277107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 120175860-C-T

43277155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120175812-C-G

43277155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120175812-C-T

http://identifiers.org/hco/5/GRCh38#43277287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120175680-C-A

43277287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120175680-C-T

http://identifiers.org/hco/5/GRCh38#43277370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120175608-C-A

43277370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175608-C-T

http://identifiers.org/hco/5/GRCh38#43277372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120175606-C-A

43277372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175606-C-T

43277491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175494-T-C

43277587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175383-C-T

43279172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175120-C-T

43279246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120175050-T-C

43279689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174624-T-C

43279833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174480-T-C

http://identifiers.org/hco/5/GRCh38#43279849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120174464-C-A

43279849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174464-C-G

43279849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174464-C-T

43279880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174428-T-C

43279893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174416-T-C

http://identifiers.org/hco/5/GRCh38#43279897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120174411-C-A

43279897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120174411-C-T

43280058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120174251-G-A

43280127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120174182-G-A

43280127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120174182-G-C

43280268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120174041-C-T

43280378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120173931-G-A

43280378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120173931-G-C

43280378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120173931-G-T

43280427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120173882-T-G

http://identifiers.org/hco/5/GRCh38#43280481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120173828-A-C

43280580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120173729-A-G

http://identifiers.org/hco/5/GRCh38#43280751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#120173558-C-A

43280751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120173558-C-G

43280815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120173496-T-A

43280815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28646
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120173496-T-C